Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1996 Jul;111(3):699–711. doi: 10.1104/pp.111.3.699

The arabidopsis ACT7 actin gene is expressed in rapidly developing tissues and responds to several external stimuli.

J M McDowell 1, Y Q An 1, S Huang 1, E C McKinney 1, R B Meagher 1
PMCID: PMC157885  PMID: 8754679

Abstract

ACT7 encodes one of the six distinct and ancient subclasses of actin protein in the complex Arabidopsis actin gene family. We determined the sequence and structure of the Arabidopsis thaliana ACT7 actin gene and investigated its tissue-specific expression and regulation. The ACT7 mRNA levels varied by 128-fold among several different tissues and organs. The highest levels of aCT7 mRNA were found in rapidly expanding vegetative organs, the lowest in pollen. A translational fusion with the 5' end of ACT 7 (1.9 kb) joined to the beta-glucuronidase reporter gene was strongly and preferentially expressed in all young, developing vegetative tissues of transgenic Arabidopsis plants. ACT7 was the only Arabidopsis actin gene strongly expressed in the hypocotyl and seed coat. Although no beta-glucuronidase expression was seen in developing ovules or immature seeds, strong expression was seen in dry seeds and immediately after imbibition in the entire seedling. ACT7 was the only Arabidopsis actin gene to respond strongly to auxin, other hormone treatments, light regime, and wounding, and may be the primary actin gene responding to external stimuli. The ACT7 promoter sequence contains a remarkable number of motifs with sequence similarity to putative phytohormone response elements.

Full Text

The Full Text of this article is available as a PDF (4.0 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. An Y. Q., Huang S., McDowell J. M., McKinney E. C., Meagher R. B. Conserved expression of the Arabidopsis ACT1 and ACT 3 actin subclass in organ primordia and mature pollen. Plant Cell. 1996 Jan;8(1):15–30. doi: 10.1105/tpc.8.1.15. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Baird W. V., Meagher R. B. A complex gene superfamily encodes actin in petunia. EMBO J. 1987 Nov;6(11):3223–3231. doi: 10.1002/j.1460-2075.1987.tb02639.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Benfey P. N., Ren L., Chua N. H. Tissue-specific expression from CaMV 35S enhancer subdomains in early stages of plant development. EMBO J. 1990 Jun;9(6):1677–1684. doi: 10.1002/j.1460-2075.1990.tb08291.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1006/abio.1976.9999. [DOI] [PubMed] [Google Scholar]
  5. Dolan L., Janmaat K., Willemsen V., Linstead P., Poethig S., Roberts K., Scheres B. Cellular organisation of the Arabidopsis thaliana root. Development. 1993 Sep;119(1):71–84. doi: 10.1242/dev.119.1.71. [DOI] [PubMed] [Google Scholar]
  6. Drouin G., Dover G. A. Independent gene evolution in the potato actin gene family demonstrated by phylogenetic procedures for resolving gene conversions and the phylogeny of angiosperm actin genes. J Mol Evol. 1990 Aug;31(2):132–150. doi: 10.1007/BF02109482. [DOI] [PubMed] [Google Scholar]
  7. Feinberg A. P., Vogelstein B. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal Biochem. 1983 Jul 1;132(1):6–13. doi: 10.1016/0003-2697(83)90418-9. [DOI] [PubMed] [Google Scholar]
  8. Fisher R. F., Egelhoff T. T., Mulligan J. T., Long S. R. Specific binding of proteins from Rhizobium meliloti cell-free extracts containing NodD to DNA sequences upstream of inducible nodulation genes. Genes Dev. 1988 Mar;2(3):282–293. doi: 10.1101/gad.2.3.282. [DOI] [PubMed] [Google Scholar]
  9. Giraudat J., Parcy F., Bertauche N., Gosti F., Leung J., Morris P. C., Bouvier-Durand M., Vartanian N. Current advances in abscisic acid action and signalling. Plant Mol Biol. 1994 Dec;26(5):1557–1577. doi: 10.1007/BF00016490. [DOI] [PubMed] [Google Scholar]
  10. Guiltinan M. J., Marcotte W. R., Jr, Quatrano R. S. A plant leucine zipper protein that recognizes an abscisic acid response element. Science. 1990 Oct 12;250(4978):267–271. doi: 10.1126/science.2145628. [DOI] [PubMed] [Google Scholar]
  11. Hemerly A. S., Ferreira P., de Almeida Engler J., Van Montagu M., Engler G., Inzé D. cdc2a expression in Arabidopsis is linked with competence for cell division. Plant Cell. 1993 Dec;5(12):1711–1723. doi: 10.1105/tpc.5.12.1711. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Hightower R. C., Meagher R. B. Divergence and differential expression of soybean actin genes. EMBO J. 1985 Jan;4(1):1–8. doi: 10.1002/j.1460-2075.1985.tb02309.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Hightower R. C., Meagher R. B. The molecular evolution of actin. Genetics. 1986 Sep;114(1):315–332. doi: 10.1093/genetics/114.1.315. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Jefferson R. A., Kavanagh T. A., Bevan M. W. GUS fusions: beta-glucuronidase as a sensitive and versatile gene fusion marker in higher plants. EMBO J. 1987 Dec 20;6(13):3901–3907. doi: 10.1002/j.1460-2075.1987.tb02730.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Jung G., Wernicke W. Patterns of actin filaments during cell shaping in developing mesophyll of wheat (Triticum aestivum L.). Eur J Cell Biol. 1991 Oct;56(1):139–146. [PubMed] [Google Scholar]
  16. Liu Z. B., Ulmasov T., Shi X., Hagen G., Guilfoyle T. J. Soybean GH3 promoter contains multiple auxin-inducible elements. Plant Cell. 1994 May;6(5):645–657. doi: 10.1105/tpc.6.5.645. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Logemann J., Schell J., Willmitzer L. Improved method for the isolation of RNA from plant tissues. Anal Biochem. 1987 May 15;163(1):16–20. doi: 10.1016/0003-2697(87)90086-8. [DOI] [PubMed] [Google Scholar]
  18. Marcotte W. R., Jr, Russell S. H., Quatrano R. S. Abscisic acid-responsive sequences from the em gene of wheat. Plant Cell. 1989 Oct;1(10):969–976. doi: 10.1105/tpc.1.10.969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. McDowell J. M., Huang S., McKinney E. C., An Y. Q., Meagher R. B. Structure and evolution of the actin gene family in Arabidopsis thaliana. Genetics. 1996 Feb;142(2):587–602. doi: 10.1093/genetics/142.2.587. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. McKinney E. C., Ali N., Traut A., Feldmann K. A., Belostotsky D. A., McDowell J. M., Meagher R. B. Sequence-based identification of T-DNA insertion mutations in Arabidopsis: actin mutants act2-1 and act4-1. Plant J. 1995 Oct;8(4):613–622. doi: 10.1046/j.1365-313x.1995.8040613.x. [DOI] [PubMed] [Google Scholar]
  21. Meagher R. B. Divergence and differential expression of actin gene families in higher plants. Int Rev Cytol. 1991;125:139–163. doi: 10.1016/s0074-7696(08)61218-8. [DOI] [PubMed] [Google Scholar]
  22. Medford J. I., Horgan R., El-Sawi Z., Klee H. J. Alterations of Endogenous Cytokinins in Transgenic Plants Using a Chimeric Isopentenyl Transferase Gene. Plant Cell. 1989 Apr;1(4):403–413. doi: 10.1105/tpc.1.4.403. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Nagao R. T., Shah D. M., Eckenrode V. K., Meagher R. B. Multigene family of actin-related sequences isolated from a soybean genomic library. DNA. 1981;1(1):1–9. doi: 10.1089/dna.1.1981.1.1. [DOI] [PubMed] [Google Scholar]
  24. Nairn C. J., Winesett L., Ferl R. J. Nucleotide sequence of an actin gene from Arabidopsis thaliana. Gene. 1988 May 30;65(2):247–257. doi: 10.1016/0378-1119(88)90461-1. [DOI] [PubMed] [Google Scholar]
  25. Roberts J. K., DeSimone N. A., Lingle W. L., Dure L., 3rd Cellular Concentrations and Uniformity of Cell-Type Accumulation of Two Lea Proteins in Cotton Embryos. Plant Cell. 1993 Jul;5(7):769–780. doi: 10.1105/tpc.5.7.769. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Rogers J. C., Rogers S. W. Definition and functional implications of gibberellin and abscisic acid cis-acting hormone response complexes. Plant Cell. 1992 Nov;4(11):1443–1451. doi: 10.1105/tpc.4.11.1443. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Schnall J. A., Quatrano R. S. Abscisic Acid Elicits the Water-Stress Response in Root Hairs of Arabidopsis thaliana. Plant Physiol. 1992 Sep;100(1):216–218. doi: 10.1104/pp.100.1.216. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Seagull R. W., Falconer M. M., Weerdenburg C. A. Microfilaments: dynamic arrays in higher plant cells. J Cell Biol. 1987 Apr;104(4):995–1004. doi: 10.1083/jcb.104.4.995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Skriver K., Olsen F. L., Rogers J. C., Mundy J. cis-acting DNA elements responsive to gibberellin and its antagonist abscisic acid. Proc Natl Acad Sci U S A. 1991 Aug 15;88(16):7266–7270. doi: 10.1073/pnas.88.16.7266. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Smyth D. R., Bowman J. L., Meyerowitz E. M. Early flower development in Arabidopsis. Plant Cell. 1990 Aug;2(8):755–767. doi: 10.1105/tpc.2.8.755. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Staiger C. J., Lloyd C. W. The plant cytoskeleton. Curr Opin Cell Biol. 1991 Feb;3(1):33–42. doi: 10.1016/0955-0674(91)90163-s. [DOI] [PubMed] [Google Scholar]
  32. Su W., Howell S. H. A Single Genetic Locus, Ckr1, Defines Arabidopsis Mutants in which Root Growth Is Resistant to Low Concentrations of Cytokinin. Plant Physiol. 1992 Aug;99(4):1569–1574. doi: 10.1104/pp.99.4.1569. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Tanzer M. M., Meagher R. B. Faithful degradation of soybean rbcS mRNA in vitro. Mol Cell Biol. 1994 Apr;14(4):2640–2650. doi: 10.1128/mcb.14.4.2640. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Thangavelu M., Belostotsky D., Bevan M. W., Flavell R. B., Rogers H. J., Lonsdale D. M. Partial characterization of the Nicotiana tabacum actin gene family: evidence for pollen-specific expression of one of the gene family members. Mol Gen Genet. 1993 Aug;240(2):290–295. doi: 10.1007/BF00277069. [DOI] [PubMed] [Google Scholar]
  35. Thompson D. M., Tanzer M. M., Meagher R. B. Degradation products of the mRNA encoding the small subunit of ribulose-1,5-bisphosphate carboxylase in soybean and transgenic petunia. Plant Cell. 1992 Jan;4(1):47–58. doi: 10.1105/tpc.4.1.47. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Uknes S., Dincher S., Friedrich L., Negrotto D., Williams S., Thompson-Taylor H., Potter S., Ward E., Ryals J. Regulation of pathogenesis-related protein-1a gene expression in tobacco. Plant Cell. 1993 Feb;5(2):159–169. doi: 10.1105/tpc.5.2.159. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Wyatt R. E., Ainley W. M., Nagao R. T., Conner T. W., Key J. L. Expression of the Arabidopsis AtAux2-11 auxin-responsive gene in transgenic plants. Plant Mol Biol. 1993 Aug;22(5):731–749. doi: 10.1007/BF00027361. [DOI] [PubMed] [Google Scholar]
  38. Zhang W., McElroy D., Wu R. Analysis of rice Act1 5' region activity in transgenic rice plants. Plant Cell. 1991 Nov;3(11):1155–1165. doi: 10.1105/tpc.3.11.1155. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Plant Physiology are provided here courtesy of Oxford University Press

RESOURCES