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. 1997 Nov;147(3):1339–1350. doi: 10.1093/genetics/147.3.1339

New Insights into the Role of the Maize Ameiotic1 Locus

I Golubovskaya 1, N Avalkina 1, W F Sheridan 1
PMCID: PMC1208256  PMID: 9383075

Abstract

In maize the am1-1 mutant allele results in both the male and female meiocytes undergoing mitosis in place of the meiotic divisions. A second mutant allele am1-praI enables both the male and female meiocytes to proceed to the early zygotene stage of meiotic prophase I before being blocked. Here we report on three new alleles that allow all male meiocytes to undergo mitosis but in female meiocytes approximately one quarter (am1-2), one half (am1-485), or all (am1-489) of them are blocked at an abnormal interphase stage. Previous analysis has shown that am1-praI is dominant to am1-1 in male meiocytes. Cytological analysis of heteroallelic combinations in female meiocytes now indicates a dominance relationship of am1-praI > am1-1 > am1-2/am1-485 > am1-489. The evidence provided by the female phenotypes of the new mutant alleles suggest that, whereas the normal am1 allele is required for the meiocytes to proceed through meiosis, a partially functional allele may be required for their diversion into a mitotic division. The partial or complete blockage of mitosis in female meiocytes carrying the new am1 alleles rules out the possibility that the mitotic division of mutant meiocytes reflects a simple default pathway for cells that cannot initiate meiosis. This locus may have a dual function.

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Selected References

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

  1. Bennett M. D. The time and duration of meiosis. Philos Trans R Soc Lond B Biol Sci. 1977 Mar 21;277(955):201–226. doi: 10.1098/rstb.1977.0012. [DOI] [PubMed] [Google Scholar]
  2. Huang B. Q., Sheridan W. F. Female Gametophyte Development in Maize: Microtubular Organization and Embryo Sac Polarity. Plant Cell. 1994 Jun;6(6):845–861. doi: 10.1105/tpc.6.6.845. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Magyar Z., Mészáros T., Miskolczi P., Deák M., Fehér A., Brown S., Kondorosi E., Athanasiadis A., Pongor S., Bilgin M. Cell cycle phase specificity of putative cyclin-dependent kinase variants in synchronized alfalfa cells. Plant Cell. 1997 Feb;9(2):223–235. doi: 10.1105/tpc.9.2.223. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Pines J. Cyclin from sea urchins to HeLas: making the human cell cycle. Biochem Soc Trans. 1996 Feb;24(1):15–33. doi: 10.1042/bst0240015. [DOI] [PubMed] [Google Scholar]
  5. Pines J. Cyclins and cyclin-dependent kinases: a biochemical view. Biochem J. 1995 Jun 15;308(Pt 3):697–711. doi: 10.1042/bj3080697. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Renaudin J. P., Colasanti J., Rime H., Yuan Z., Sundaresan V. Cloning of four cyclins from maize indicates that higher plants have three structurally distinct groups of mitotic cyclins. Proc Natl Acad Sci U S A. 1994 Jul 19;91(15):7375–7379. doi: 10.1073/pnas.91.15.7375. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Sheridan W. F., Avalkina N. A., Shamrov I. I., Batygina T. B., Golubovskaya I. N. The mac1 gene: controlling the commitment to the meiotic pathway in maize. Genetics. 1996 Mar;142(3):1009–1020. doi: 10.1093/genetics/142.3.1009. [DOI] [PMC free article] [PubMed] [Google Scholar]

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