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. 2023 Mar 29;14:1753. doi: 10.1038/s41467-023-37408-w

Fig. 1. Transcriptionally active isoform of RNA polymerase II, Ser2P, is enriched in pachynema and diplonema.

Fig. 1

ac Immunofluorescence staining on spread meiotic spermatocyte preparations from wild-type C57Bl/6 mice using antibodies against SYCP3 (green) and Pol II (a), Ser5P (b), and Ser2P (c) (magenta). Leptonema (L), zygonema (Z), pachynema (P), diplonema (D), and diakinesis (Dia) staged spermatocytes are defined by SYCP3 morphology. The X and Y chromosomes are outlined in white. Arb. units = arbitrary units. df Quantification of signal intensity for Pol II, Ser5P, and Ser2P immunofluorescence staining in wild-type spermatocytes. Average intensity is shown, and error bars represent 95% confidence intervals. Samples were obtained from three 3-month-old mice. Source data are provided as a Source data file. d n = 606 prophase I cells. e There was no significant difference in the fluorescence intensity of Ser5P between prophase I substages. n = 586 prophase I cells. f n = 677 prophase I cells. g Radioactive nuclear run-on results comparing the relative levels of nascent transcription between leptonema/zygonema (LZ), pachynema (P), diplonema (D), and round spermatids (RS). Average relative transcriptional activity is shown, and error bars represent standard deviation. Source data are provided as a Source data file. dg *p-value = 0.012, **p-value = 0.0056, ****p-value <0.0001, one-way ANOVA with the post hoc Tukey’s multiple comparison’s test.