Abstract
The Fly-CURE is a genetics-focused multi-institutional Course-Based Undergraduate Research Experience (CURE) that provides undergraduate students with hands-on research experiences within a course. Through the Fly-CURE, undergraduate students at diverse types of higher education institutions across the United States map and characterize novel mutants isolated from a genetic screen in Drosophila melanogaster. To evaluate the impact of the Fly-CURE experience on students, we developed and validated assessment tools to identify students’ perceived research self-efficacy, sense of belonging in science, and intent to pursue additional research opportunities. Our data show gains in these metrics after completion of the Fly-CURE across all student subgroups analyzed, including comparisons of gender, academic status, racial and ethnic groups, and parents’ educational background. Importantly, our data also show differential gains in the areas of self-efficacy and interest in seeking additional research opportunities between Fly-CURE students with and without prior research experience, illustrating the positive impact of research exposure (dosage) on student outcomes. Altogether, our data indicate that the Fly-CURE experience has a significant impact on students’ efficacy with research methods, sense of belonging to the scientific community, and interest in pursuing additional research experiences.
Keywords: Drosophila, CURE, undergraduate research, pedagogy, genetics, STEM, education
INTRODUCTION
As undergraduate STEM education continues to evolve and make improvements that facilitate the training of scientists from diverse backgrounds, it is becoming increasingly apparent that an authentic research experience is key for promoting student persistence within STEM majors and for adequate preparation for future scientific careers. There has been a national call for all STEM majors to have such an experience during their undergraduate education (1, 2), however, a significant challenge to this call is simple logistics. While some undergraduates do participate in a traditional apprentice-based research experience, there is not enough research lab capacity to accommodate all undergraduate STEM majors (3). One response to limited research opportunities has been to incorporate authentic research experience(s) into the curriculum. Such courses, often referred to as CUREs (Course-based Undergraduate Research Experiences), provide a research experience to a larger number of students (approximately 20–25 students per faculty or teaching assistant mentor) within a single iteration (3–5). Several CURE-type endeavors have been developed and, consequently, have provided research opportunities to a far greater number of STEM undergraduates than would have been possible through mentored bench research alone (5–11).
CURE participation positively impacts science education in several ways. In comparison with traditional apprenticeships, CUREs not only reach more students, but also represent a more inclusive approach to research (3, 12). Student participation in CUREs has been shown to enhance critical thinking skills (10, 13), increase learning gains , bolster scientific identity (14, 15), and increase interest in science and scientific research (16). Each of these outcomes is likely an important factor driving the positive correlation between student participation in CUREs and increased STEM retention rates, including for underrepresented minority students (11, 17, 18).
Faculty, departments, and the scientific community at large can also be positively impacted by implementing CURE pedagogies. Faculty at Primarily Undergraduate Institutions (PUIs) typically have a heavy teaching requirement (teaching 3–4 classes per semester is not uncommon) that often comes with the additional expectation of research productivity (19). CUREs provide such faculty with an opportunity to combine teaching and research into a single endeavor that can, when properly structured and implemented, produce publishable work (both research data collected/analyzed by the students and pedagogical data measuring the impact on students) (16, 17, 20, 21). However, setting up a successful CURE comes with many challenges, the largest of which is typically the identification of a research project that is feasible for undergraduates working within the confines of a laboratory course (meeting 1–2 times per week, 3–5 hours total), budget-friendly, and longitudinally sustainable. The implementation of CUREs by regional and national consortia has been successful in overcoming many of these challenges. Efforts such as Science Education Alliance (SEA-PHAGES), Genomics Education Partnership (GEP), and Small World Initiative, have had success with CURE implementation at multiple sites, due in part to offering established, ready-to-go projects that entice faculty participation by reducing the burden of identifying a suitable research project and developing the infrastructure to support these projects (22–24). Not only does this approach provide research opportunities for more students, but it also increases the amount of valuable undergraduate-generated data. In addition, faculty and student participants are typically authors on research papers that include their contributing data. Here we describe a new CURE consortium called Fly-CURE that utilizes Drosophila melanogaster as a research model in undergraduate genetics laboratory courses.
The Fly-CURE was established in 2012 at the University of Detroit Mercy and centers on characterizing and mapping novel EMS-induced mutations isolated in a genetic screen for genes that regulate cell growth and cell division within the developing Drosophila eye (25). In the Fly-CURE, students start with an uncharacterized mutant and, in its analysis, learn about and utilize a variety of techniques commonly taught in more traditional undergraduate genetics laboratory courses. The Fly-CURE curriculum includes, but is not limited to classical Mendelian genetics, molecular genetics, and bioinformatics. Over the last ten years, students participating in the Fly-CURE have characterized over twenty novel Drosophila mutations, which have been published in eleven publications and included 581 student co-authors (26–36). Currently, the Fly-CURE is being taught at over twenty institutions across the United States. The institutional diversity of the Fly-CURE consortium has allowed us to measure the impact of the Fly-CURE pedagogy on a variety of student attitudes, including their sense of belonging in STEM, research competency, and intent to continue toward a STEM career. We also evaluated the effect of dosage on these metrics, where dosage refers to research experiences that a student participated in prior to participation in the Fly-CURE research project. Assessing the impact of research experience “dosage” on STEM undergraduates participating in the Fly-CURE consortium may shed light upon whether there is a critical number of research experiences that impact students’ retention and ultimate success in STEM fields.
METHODS
Fly-CURE consortium: institutions, faculty, and student participants
Pre- and post-survey data were gathered from 480 Fly-CURE students over three academic years: 2019–2020, 2020–2021, and 2021–2022. The demographics of the participating schools and students are detailed in Appendix 1 and shown in Figure 2. In the years of data collection and in the data presented, there were 15 faculty who implemented the Fly-CURE across 14 institutions.
All participating students were asked to complete a voluntary online survey before beginning (pre-course) and after completing (post-course) a Fly-CURE course offering (see Figure 1A for workflow). Approval to assess students was obtained by each participating institution from their Institutional Review Board. After each semester, responses were collected and analyzed by SPEC Associates (Southfield, MI), an independent analytics firm specializing in education and learning. Confidentiality was maintained by providing each instructor with a unique link to the online surveys that could be distributed to students. SurveyMonkey was the online platform used, with completed surveys being directly received by SPEC Associates without the instructors’ ability to see responses. The components of the pre- and post-course surveys used for this study are available in Appendix 2.
From the 895 students invited to participate in the surveys, we received 740 completed pre-course surveys and 683 completed post-course surveys. Only data in which students took both the pre- and post-course surveys were used in our analysis (69% of surveys were pre-/post-test matched). Pre- and post-survey responses were matched based on answers to non-identifying questions such as childhood home address. Student attentiveness was also assessed using one inattentive item on both the pre- and post-survey. Students who did not respond accordingly were eliminated from the analysis. Ternovski and Orr provide evidence that survey respondents who are inattentive also provide less reliable demographic data and are systematically different from attentive respondents (37). Following analysis for student attentiveness and pre-/post-test pairing, 65% of surveys were included in our current study. The number of surveys used in each comparative analysis differed because some students responded to only a subset of the survey items.
Participants identified their gender as female (69%), male (28%), their gender was not listed (1%), or they preferred not to say (2%). Participants were from ethnic or racial groups classified by the NSF as underrepresented in STEM (27%) and groups not considered underrepresented in STEM (73%). Demographic groups who were considered underrepresented in STEM were the following: Native Hawaiian or other Pacific Islander (original peoples), American Indian or Alaskan Native, Black or African American (including African and Caribbean), and Hispanic or Latino. Demographic groups who were not considered underrepresented in STEM included students who identified as White, Asian (including subcontinent and Philippines), and of Middle Eastern descent. Participants also reported whether either parent attended any college (continued-generation college students, 71%) or neither parent attended any college (first-generation college students, 29%). Moreover, student participants ranged in academic year (4% first-year students, 34% second-year students, 31% third-year students, 29% fourth-year students, and 2% students who already had a bachelor’s degree). For our study, we combined first- and second-year students (38% of participants) and third-year students and beyond (62%).
Measure of research experience and dosage
Pre-course surveys asked participants to report any research-associated experiences prior to the Fly-CURE. Refer to pre-survey question 7 (Appendix 2) for the specific experiences listed. Students who chose “yes” to any of these experiences were considered as having prior research exposure, while those who did not choose “yes” to any of these questions were considered as not having prior research exposure.
Fly-CURE outcome measures
Survey items for assessing research self-efficacy and sense of belonging were adapted from items used in the evaluation of the National Institutes of Health’s Building Infrastructure Leading to Diversity (BUILD) initiative. This retrospective pre-/post-survey method of measuring outcomes is commonly used when there is a possibility that students’ understanding of the constructs, such as what a research-intensive science laboratory course is, changes as a result of participating in the course and eliminates the possibility of a response shift bias in the data (38). For each evaluated outcome, students self-reported their pre- and post-course confidence or agreement with specific matrices using a 1–5 Likert scale.
Research self-efficacy:
Pre- and post-course surveys asked students to report their perceived abilities and confidence for eight statements (Appendix 2, pre-survey question 8 and post-survey question 4). The scores from all eight questions were added together, resulting in a scale ranging from 8 to 40. Psychometric analysis of the pre- and post-course survey data revealed that this scale had a coefficient alpha of 0.918 for the pre-survey and 0.975 for the post-course survey, indicating these items measure the same construct.
Sense of belonging in science:
Pre- and post-course surveys asked students to report their perceived agreement with four statements (Appendix 2, pre-survey question 9 and post-survey question 5). To determine scale scores, the results from all four questions were added together, resulting in a scale of 4 to 20. Psychometric analysis revealed that this scale had coefficient alphas of 0.863 and 0.935 for the pre- and post-course surveys, respectively.
Intent to pursue additional research opportunities:
Post-course surveys asked participants to report their perceived intentions before and after taking the course. Students reported their likelihood to do each of the following: (i) enroll in another research-intensive science laboratory course; (ii) pursue or continue independent research in a science laboratory; (iii) pursue a career as a scientist (Appendix 2, post-survey questions 1–3). The scores from all three questions were analyzed separately or added together on a scale of 3 to 15. Psychometric analysis showed that this scale had a coefficient alpha of 0.861 for the pre-survey and 0.789 for the post-course survey.
Statistical analyses
Independent groups and paired t-tests were used to assess the statistical significance of differences in the means within the same students from pre- to post-course (paired t-tests) and between different groups of students (independent groups t-tests). Levene’s Test for Equality of Variances was used to test for homogeneity of variance.
The mean scores for the three outcome scales were calculated in two ways: the scale score means and the gain score mean. Two scale score means are calculated for each outcome, a pre- and a post-course scale score mean, representing the average of student scale scores. The scale score mean may underestimate change because some students may have rated themselves the highest possible score on the pre-course survey. If they also rate themselves the highest possible score on the post-course survey, the difference between the pre- and post-course scores is zero. These students may have rated themselves even higher on the post-course survey, but the maximum possible score presented a ceiling for them. Thus, the scale score mean includes these zeros and deflates the mean score for the group. To account for this, a second mean score was calculated using the normalized gain score. The gain score removes students with the highest possible pre-course score from the analysis and examines the degree of change among students who could change because they did not reach the ceiling score on the pre-course survey (39). The equation used to calculate the normalized gain score is: Normalized Gain = (Post-score – Pre-score)/(Maximum possible score - Pre-score). The data presented herein include both the scale score mean and the mean gain scores for all statistical comparisons.
RESULTS
The Fly-CURE focuses on the genomic mapping and phenotypic characterization of EMS-induced mutant lines involved in Drosophila eye development
At the beginning of each semester, all required Drosophila stocks were shipped to participating institutions. Drosophila mutant stocks contain previously generated EMS-induced mutations on the right arm of chromosome 2 (2R) (25). These mutations were previously identified based on homozygous recessive lethality and a growth-associated phenotype in the Drosophila eye when cell death is also blocked, but the genomic locus of the mutations is unknown (26, 27, 29–35). The identified mutants serve as the basis for phenotypic eye characterization, complementation mapping, and molecular analysis modules of the Fly-CURE (Figure 1A,B).
The Fly-CURE is a lab research project that includes both an initial “Discovery Phase” and a subsequent “Inquiry Phase” (Figure 1A). An initial pre-survey (Appendix 2) is first completed by all participating students to gather information about general student demographics, prior research experience, research self-efficacy, and sense of belonging in science. Students then typically complete an initial “Discovery Phase” of the project to characterize the eye tissue growth phenotype caused by the EMS-induced mutation and use complementation mapping of the lethal phenotype with a series of defined chromosomal deletions (40) to identify the genomic locus where the mutation responsible for the observed phenotype may be found. All recessive lethal EMS-induced mutations being investigated, as well as the chromosomal deficiencies used for complementation mapping, are maintained as heterozygotes using a second chromosome balancer causing curly wings (a dominant phenotypic marker; Figure 1A). Therefore, for crosses between the Drosophila mutant stock and stocks containing chromosomal deficiencies along 2R, students use stereomicroscopes to easily score for the presence (complementation) or absence (failure to complement) of straight-winged flies (those carrying the mutation and deficiency) among the progeny. Since the chromosomal deletions used in the first round of complementation mapping are relatively large and often lack several dozen to hundreds of genes (40), a second round of complementation tests with smaller deletions and/or chosen null alleles of individual genes within the specific genomic region identified in the first round of complementation mapping can be utilized to identify a smaller region where the mutation might be located. Once non-complementing deficiencies are identified, this concludes the “Discovery Phase” of the CURE.
During the “Inquiry Phase”, students develop hypotheses about candidate genes within the genomic region that fails to complement lethality of the mutation. Student-derived hypotheses usually focus on why mutations within a specific gene might lead to the observed eye tissue phenotype or recessive lethality. Typically, students choose genes that have been previously annotated as being involved in cellular growth control, apoptosis, the cell cycle, or similar processes. In some cases, the EMS mutation fails to complement a mutant allele of a specific gene by the second round of crosses (29, 32, 34, 35), allowing students to focus their hypothesis generation and subsequent molecular analyses on a single gene. Students then isolate genomic DNA from the mutant and control fly stocks, design PCR primers, and amplify a small (500–1000 nucleotide) region of their chosen gene. The sequence of the amplified region from both the mutant and control stocks is then determined by Sanger sequencing to identify possible differences between the heterozygous mutant stock and the wild-type control. Then, students use bioinformatics approaches to understand protein structure and/or evolutionary conservation of the candidate gene and often present their findings to the rest of the class. Finally, students analyze, summarize, and connect the data acquired. Different pedagogical assessments are used across the consortium, including formal lab reports, poster presentations, and micropublication-style manuscripts. At the end of the semester, a post-survey was completed to assess whether the semester-long Fly-CURE impacted students’ sense of belonging within the scientific community, feelings of self-efficacy in research, and motivation to pursue other future research experiences or STEM careers.
Fly-CURE is a modular research experience that can be implemented in a variety of laboratory classes
The modular nature of Fly-CURE allows for components to be organized or omitted to meet the learning objectives and scheduling variability of different courses (Figure 1B). For example, most courses that have implemented the Fly-CURE have been upper-level genetics classes that also contain a laboratory component (Figure 1C, n=9). These combined lecture and lab courses, along with stand-alone genetics laboratory courses that lack a separate lecture component (n=4), typically utilize all modules of the Fly-CURE (Figure 1B, version 1). However, the Fly-CURE has also been implemented in Introductory Biology (n=1), a sophomore-level Molecular Biology course (n=1), and Anatomy and Physiology (n=1). In these non-genetics-centered classes, other variations of the Fly-CURE have been implemented that lack one or more of the modules contained in Fly-CURE version 1 (Figure 1B). Thus, while Fly-CURE has been mostly implemented in genetics courses, its adaptability and student-focused nature have allowed a wide variety of courses to participate in this course-embedded research experience.
While the modularity and adaptability of the Fly-CURE have allowed for its implementation in a variety of courses, we also wanted to assess whether faculty using this CURE could do so successfully without prior research experience with Drosophila. We surveyed faculty who had implemented the Fly-CURE and found that only slightly more than half (53%, n=8), had previously trained as a graduate student or postdoctoral fellow in a research lab where Drosophila melanogaster was utilized as a genetic model organism (Figure 1D). Together, these data suggest that Fly-CURE can be widely implemented in a variety of courses and that extensive prior training or experience in a Drosophila research lab by the faculty instructor is not a requisite for Fly-CURE implementation.
The Fly-CURE provides research experiences at a range of institutions and for a broad spectrum of student participants
One motivation for the development of the Fly-CURE was to establish opportunities for collaboration between faculty and students at different institutions. Faculty were recruited to participate in Fly-CURE through a variety of methods, including discussions at conferences, social media, and word-of-mouth. The cohort of faculty collaborating on the Fly-CURE spanned several types of institutions (Figure 2A). Approximately equal numbers of faculty at Primarily Undergraduate Institutions (PUIs, n=6) and non-R2 graduate degree-granting institutions (n=5) have implemented the Fly-CURE into at least one course. In addition, the Fly-CURE has been implemented at R2 institutions (n=3) and at a community college (n=1), where undergraduate research experiences are typically limited due to a variety of factors including teaching load and institutional resources (3, 41, 42). Approximately 20% of institutions where the Fly-CURE has been taught over the last three years are also classified as Minority Serving Institutions (MSIs) (Figure 2B). Regular virtual meetings between participating faculty serve to foster collaboration between classes characterizing the same Drosophila mutation and have also culminated in eight collaborative micropublications consisting entirely of student-generated data (27, 29–35).
Among all students who have participated in the Fly-CURE, 27% self-identify as belonging to a demographic group underrepresented in STEM (Figure 2C) and 29% of students are first-generation college students (Figure 2D). In addition, only slightly more than half (52.5%) of students had any research exposure before the Fly-CURE (Figure 2E). Of the students who previously participated in a research experience, most had participated in a course-based research experience (Figure 2F), while only 26% of students had participated in a mentored apprenticeship-style research experience. Given the significant positive impacts that research experiences have on undergraduate STEM majors (43) and the dearth of mentored research experiences typically available to many undergraduate students, these data suggest that CUREs provide an important alternative to traditional apprentice-style research positions. While first-year undergraduate research experiences have been shown to be particularly important for the retention of STEM majors (44), the correlation between the number of research experiences a student participates in and student outcomes has been less well-studied. In particular, course-embedded research experiences like the Fly-CURE provide an additional “dose” of research to a large number of students, and in so doing, further promote student self-efficacy in research, sense of belonging in the scientific community, and pursuit of STEM careers.
Impact of the Fly-CURE on student self-efficacy in research
To evaluate the impact of the Fly-CURE experience on students’ research self-efficacy, sense of belonging in science, and student interest in pursuing additional research experiences, pre- and/or post-course surveys were used to ask students about their confidence or level of agreement with multiple statements focused on these areas. Likert scale responses for questions focused on each metric were tallied to generate scale scores. Lower scale scores represent less confidence or agreement with associated statements, while higher scale scores represent students who reported more confidence or agreement with included statements.
As a first measurement of Fly-CURE effectiveness, we analyzed students’ sense of research self-efficacy. Students ranked their confidence in response to eight statements pertaining to this metric on pre- and post-course surveys (see Methods and Appendix 2). Students reported increased self-efficacy in research from pre-course to post-course, shown as an increase in scale score means (Figure 3A) and as a mean gain score (Figure 3B). We were also interested in whether the Fly-CURE closed gaps in research self-efficacy for specific student subgroups that are underrepresented in STEM, thereby providing a path to increased diversity in STEM. Interestingly, female students reported lower confidence in research pre-course (28.0 for females, 29.2 for males) and surpassed males in reported self-efficacy post-course (31.5 for females, 31.0 for males) (Figure 3C), resulting in a gain in research self-efficacy for both male and female students (Figure 3D). Although all student subgroups reported significant gains in their self-efficacy in research post-course, there were no statistically significant differences in the degree of reported gains in research self-efficacy between students in the evaluated subgroups, including race and ethnicity (Figure 3E, Supplemental Figure 1A,B), education background of parents (Figure 3E, Supplemental Figure 1C,D), and academic year (Supplemental Figure 1E,F).
Impact of the Fly-CURE on student sense of belonging in the scientific community
Pre- and post-course surveys were also used to evaluate the effectiveness of the Fly-CURE in increasing student sense of belonging in science by asking students to rate their level of agreement with four statements (see Methods and Appendix 2). Pre- and post-course sense of belonging scales were generated by adding each student’s ratings on the four items.
Similar to their reported gains in research self-efficacy, students reported an increased sense of belonging in the scientific community post-course compared to pre-course. This is shown as scale score means (Figure 4A) and as a mean gain score (Figure 4B). We also compared student subgroups in several demographic categories and found that although all student subgroups reported gains in their feelings of belonging in science post-course, there were no statistically significant differences in the degree of reported gains between subgroups in each evaluated category, including gender (Figure 4C,D), race and ethnicity (Figure 4E, Supplemental Figure 2A–B), education background of parents (Figure 4E, Supplemental Figure 2C,D), and academic year (Supplemental Figure 2E,F). These data suggest that students from underrepresented backgrounds participating in Fly-CURE make similar gains as their peers. It is worth noting that similar to research self-efficacy, female participants reported a lower sense of belonging in science pre-course (12.2) compared to males (13.1), but yet reached a score similar to males post-course (13.8 for females, 14.0 for males) (Figure 4C). This suggests that the Fly-CURE experience allows female students to increase their perceived sense of belonging in science, thereby narrowing the gender gap in STEM.
Impact of the Fly-CURE on student intention to pursue additional research opportunities
To evaluate the effectiveness of the Fly-CURE in increasing student intention to pursue additional research-associated experiences, post-course surveys asked participants to rate their perceived likelihood to seek out additional research opportunities before and after taking the course for three questions (see Methods and Appendix 2). Much like the reported gains in research self-efficacy and sense of belonging in science, students also reported a perceived increase in their intention to pursue additional research experiences after completing the Fly-CURE. This can be observed as scale score means (Figure 5A), as a mean for each type of experience evaluated (Figure 5B), and as a mean gain score for each type of experience (Figure 5C). It is worth noting that all student subgroups analyzed tend to start at a similar level of perceived intent to pursue the experiences proposed before the course and have a similar level of intent after the course (Supplemental Figure 3). Altogether, these data highlight the positive impact that the Fly-CURE has on encouraging confidence, belonging, and persistence in science for students who participate in a CURE during their undergraduate education.
Impact of the Fly-CURE on students with and without previous research experiences
While much of our data support previously reported impacts that CUREs have on student gains (42, 48), thereby highlighting the effectiveness of the Fly-CURE experience for students, we were also interested in evaluating the impacts of the Fly-CURE on students with or without research experience prior to taking a Fly-CURE course. In a pre-course survey, students were asked which specific research experiences, if any, they had prior to beginning the Fly-CURE project (see Methods and Appendix 2). Approximately 53% of students reported having had research experience of some kind before starting the Fly-CURE (Figure 2E).
Students with and without prior research experience reported gains in self-efficacy in research (Figure 6A) and sense of belonging in the scientific community (Figure 6C) after completing the Fly-CURE. Interestingly, however, students without prior research experience reported a greater gain in research self-efficacy after the Fly-CURE, suggesting that the Fly-CURE serves as a valuable research experience for those students and makes strides in increasing their confidence in conducting research (Figure 6B). On the contrary, students with and without prior research experience did not exhibit differential gains in their sense of belonging to the scientific community (Figure 6D). It is important to note, however, that the mean sense of belonging score for students without prior research experience post-course (13.3) surpassed the pre-course score for students with prior research experience (13.0) (Figure 6C). This indicates that the research experience component of the Fly-CURE increases students’ sense of belonging in science from baseline and suggests that there may be a dose-dependent relationship between the number of research experiences a student has and students’ sense of belonging in the scientific community.
Next, we evaluated whether the Fly-CURE had differing impacts on students’ intention to pursue additional research opportunities depending on whether students entered the CURE with or without prior research experience. In particular, we questioned whether participating in at least one research experience before the Fly-CURE resulted in a greater increase in students’ intent to seek out future research experiences compared to those without prior research experience. We found that although interest in gaining additional future experiences increased for all students (Figure 5A, Supplemental Figure 3), differential outcomes were observed, depending on the type of experience and whether students had research experience before taking the Fly-CURE course (Figure 6E–G). When students were asked whether they were interested in enrolling in another research-intensive laboratory course such as a CURE, students with prior research experience exhibited a greater gain in intent to pursue this experience, as shown by the gain score mean post-Fly-CURE compared to pre-Fly-CURE (P ≤ 0.05) (Figure 6E; scale score mean data in Supplemental Figure 4A). Similarly, students with prior research experience reported a greater gain in their intent to pursue or continue independent research in a scientific research laboratory than students without prior research experience (P ≤ 0.05) (Figure 6F; Supplemental Figure 4B). These data support the hypothesis that increased dosage in research experiences positively correlates with increases in student interest to persist in research. The only category in which students with and without prior research experience did not show differential outcomes was for intention to pursue a career as a scientist (Figure 6G; Supplemental Figure 4C). Regardless of the extent of prior research experience, students reported a very similar increase in intent to become scientists post-Fly-CURE as they did before Fly-CURE, suggesting that additional exposure to research does not significantly increase, beyond the initial positive impact, students’ interest to pursue a career in STEM.
Altogether, our data show that all students, regardless of demographic profile and previous exposure to research, show an increase in research self-efficacy, sense of belonging in science, and interest in pursuing additional research experiences after taking a Fly-CURE course. In addition, students without prior research experience show a statistically significant gain in self-efficacy compared with students with prior research experience; while students with prior experience in research show a statistically significant gain in interest to seek out additional research opportunities, but no significant increase in intent to pursue a career as a scientist.
DISCUSSION
The Fly-CURE is a versatile authentic research experience that can be implemented in a modular fashion across course and/or institution types, and without requiring prior experience with Drosophila melanogaster (Figure 1B–D and Figure 2A,B). Thus, the Fly-CURE consortium is a large and diverse sample for measuring the impact of course-embedded research on student attitudes regarding self-efficacy in research, sense of belonging in science, intent to pursue additional research experiences, and the impact of previous research experiences (dosage) on these metrics. Prior studies have suggested that increased time spent on a task and research dosage positively impact student outcomes and persistence in STEM (45, 46). However, it has been suggested that persisting in science may require “a commitment of 10 or more hours per week over two or more semesters of faculty-mentored research” (3, 45). Therefore, we investigated the relationship between research exposure and its impacts on students’ retention, belonging, and confidence in STEM.
Overall, gains were reported by Fly-CURE students for scientific self-efficacy and sense of belonging, as well as for their intent to persist in STEM. Our analysis shows that all participating students, including groups considered underrepresented in STEM, females, and first-generation college students, reported increased confidence in research-associated skills (Figure 3 and Supplemental Figure 1), sense of belonging in science (Figure 4 and Supplemental Figure 2), and interest in pursuing additional research experiences (Figure 5 and Supplemental Figure 3) after the Fly-CURE. These are gains previously reported by others and our data supports the growing notion that CUREs are inclusive and have a positive impact on undergraduate STEM education (10, 11, 13–17).
Further, the fact that Fly-CURE is successfully implemented by faculty at a wide range of institutions (e.g., PUI, CC, MSI, and R2), a variety of courses, and by faculty without prior experience with Drosophila demonstrates the adaptable nature of the Fly-CURE. This also exemplifies the effectiveness of the Fly-CURE consortium for providing authentic research experiences for an increased number of STEM students. Traditional apprentice-based research experiences are often limited in availability, budget, and/or capacity, rendering the need for course-based experiences. However, one of the barriers to starting a CURE is having a project that is sustainable and feasible within the confines of an undergraduate curriculum. Additional barriers to CURE implementation exist for some institutional types such as community colleges (47). Nevertheless, community college students have comparable knowledge and perceived outcomes gains as non-community college counterparts when engaging in centrally supported CUREs, demonstrating the need for these research experiences to be accessible to all students (41, 42). The versatility associated with the modular nature of experiments in the Fly-CURE, as well as the diverse range of institutions at which the Fly-CURE has been implemented successfully, highlight its value for both students and curricula.
While other research endeavors have looked at dosage in terms of how much time a researcher spends on a single project (45, 46), we were able to investigate whether a separate previous research experience had an impact on changes in attitude resulting from the Fly-CURE (Figure 6 and Supplemental Figure 4). There were two lessons that emerged from our findings that could impact how undergraduate STEM departments incorporate research into their curriculum. The first is that students with no self-reported previous research experience demonstrated gains in both research self-efficacy and sense of belonging after a single semester of research (Figure 6A–D). Perhaps not surprisingly, these students reported a more significant gain in research self-efficacy than their classmates who had previous research experience (Figure 6A,B). This may be one of the most promising aspects of the Fly-CURE as a pedagogy to broaden participation in institutions where research opportunities are especially limited, such as two-year institutions with the most diverse student populations. Additionally, students with prior research experience reported a more significant gain in their intent to enroll in another research-intensive course and pursue independent research in a science lab (Figure 6E,F), highlighting a correlation between increased dosage and interest to persist in research. However, both students with and without prior research experience showed similar gains in their intent to pursue a career as a scientist (Figure 6G), suggesting that career plans might be less subjective to research exposure dosage. It is worth noting that the future career plans for many Fly-CURE participants might be in STEM-related careers, such as health professions, but not necessarily in laboratory research. Thereby, we predict that most respondents perceived a “career as a scientist” as a bench or field scientist, rather than a health-centered career. In the future, it would be enlightening to offer more specific career avenues to better appreciate the impact of the Fly-CURE on participants’ career interests.
Overall, these data show that participation in the Fly-CURE, as a single research experience, increases these metrics, even if this CURE is the student’s first research experience. Second, those students who had previous research experience also had statistically significant gains after completing the Fly-CURE, suggesting that all students have room to grow for the metrics analyzed in the second (or beyond) research experience. From our data, we cannot conclude how many research experiences would saturate these reported gains; however, we think it is reasonable to hypothesize that additional research experiences would result in additional gains in these areas. Future studies should specifically evaluate the critical number of research experiences associated with these and other student outcomes. Nonetheless, our data support previous evidence on the impacts of CUREs, thereby further underlining the importance for undergraduate STEM departments to incorporate one (or more) research experiences into the standardized curriculum.
Supplementary Material
ACKNOWLEDGEMENTS
We thank all Fly-CURE students who completed surveys and contributed to this work, as well as Alexandra Peister at Morehouse College and Clare Kron, Elizabeth Taylor, Hemin Shah, and Sandesh Pandit at NIU. Thanks also to the Bloomington Drosophila Stock Center, especially Kevin Cook and Cale Whitworth, for generously providing stocks. Figure 1A was made using BioRender.com. The research was supported by NSF IUSE grant 2021146 to JDK, KLB, JS, and ADV-M and NIH ReBUILDetroit grants UL1GM118982, TL4GM118983, and RL5GM118981 to JDK, VLS, and MAH.
Sources of support:
NSF IUSE grant 2021146 to JDK, KLB, JS, and ADV-M; NIH ReBUILDetroit grant UL1GM118982, TL4GM118983, and RL5GM118981 to JDK, MAH, and VLS
Footnotes
Conflict of Interest Notification
The authors certify that they have no conflicts of interest to disclose.
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