Skip to main content
Genetics logoLink to Genetics
. 1995 Dec;141(4):1473–1481. doi: 10.1093/genetics/141.4.1473

Mutational Analyses of Fs(1)ya, an Essential, Developmentally Regulated, Nuclear Envelope Protein in Drosophila

J Liu 1, K Song 1, M F Wolfner 1
PMCID: PMC1206880  PMID: 8601487

Abstract

The fs(1)Ya protein (YA) is an essential, maternally encoded, nuclear lamina protein that is under both developmental and cell cycle control. A strong Ya mutation results in early arrest of embryos. To define the function of YA in the nuclear envelope during early embryonic development, we characterized the phenotypes of four Ya mutant alleles and determined their molecular lesions. Ya mutant embryos arrest with abnormal nuclear envelopes prior to the first mitotic division; a proportion of embryos from two leaky Ya mutants proceed beyond this but arrest after several abnormal divisions. Ya unfertilized eggs contain nuclei of different sizes and condensation states, apparently due to abnormal fusion of the meiotic products immediately after meiosis. Lamin is localized at the periphery of the uncondensed nuclei in these eggs. These results suggest that YA function is required during and after egg maturation to facilitate proper chromatin condensation, rather than to allow a lamin-containing nuclear envelope to form. Two leaky Ya alleles that partially complement have lesions at opposite ends of the YA protein, suggesting that the N- and C-termini are important for YA function and that YA might interact with itself either directly or indirectly.

Full Text

The Full Text of this article is available as a PDF (4.5 MB).

Selected References

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

  1. Allis C. D., Waring G. L., Mahowald A. P. Mass isolation of pole cells from Drosophila melanogaster. Dev Biol. 1977 Apr;56(2):372–381. doi: 10.1016/0012-1606(77)90277-9. [DOI] [PubMed] [Google Scholar]
  2. Berg J. M. Zinc fingers and other metal-binding domains. Elements for interactions between macromolecules. J Biol Chem. 1990 Apr 25;265(12):6513–6516. [PubMed] [Google Scholar]
  3. Boswell R. E., Mahowald A. P. tudor, a gene required for assembly of the germ plasm in Drosophila melanogaster. Cell. 1985 Nov;43(1):97–104. doi: 10.1016/0092-8674(85)90015-7. [DOI] [PubMed] [Google Scholar]
  4. Churchill M. E., Suzuki M. 'SPKK' motifs prefer to bind to DNA at A/T-rich sites. EMBO J. 1989 Dec 20;8(13):4189–4195. doi: 10.1002/j.1460-2075.1989.tb08604.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. DOANE W. W. Completion of meiosis in uninseminated eggs of Drosophila melanogaster. Science. 1960 Sep 9;132(3428):677–678. doi: 10.1126/science.132.3428.677. [DOI] [PubMed] [Google Scholar]
  6. Freeman M., Glover D. M. The gnu mutation of Drosophila causes inappropriate DNA synthesis in unfertilized and fertilized eggs. Genes Dev. 1987 Nov;1(9):924–930. doi: 10.1101/gad.1.9.924. [DOI] [PubMed] [Google Scholar]
  7. Freeman M., Nüsslein-Volhard C., Glover D. M. The dissociation of nuclear and centrosomal division in gnu, a mutation causing giant nuclei in Drosophila. Cell. 1986 Aug 1;46(3):457–468. doi: 10.1016/0092-8674(86)90666-5. [DOI] [PubMed] [Google Scholar]
  8. Furukawa K., Hotta Y. cDNA cloning of a germ cell specific lamin B3 from mouse spermatocytes and analysis of its function by ectopic expression in somatic cells. EMBO J. 1993 Jan;12(1):97–106. doi: 10.1002/j.1460-2075.1993.tb05635.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Glover D. M., Raff J., Karr T. L., O'Neill S. L., Lin H., Wolfner M. F. Parasites in Drosophila embryos. Nature. 1990 Nov 8;348(6297):117–117. doi: 10.1038/348117a0. [DOI] [PubMed] [Google Scholar]
  10. Judd B. H., Young M. W. An examination of the one cistron: one chromomere concept. Cold Spring Harb Symp Quant Biol. 1974;38:573–579. doi: 10.1101/sqb.1974.038.01.061. [DOI] [PubMed] [Google Scholar]
  11. Kalb J. M., DiBenedetto A. J., Wolfner M. F. Probing the function of Drosophila melanogaster accessory glands by directed cell ablation. Proc Natl Acad Sci U S A. 1993 Sep 1;90(17):8093–8097. doi: 10.1073/pnas.90.17.8093. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Krohne G., Benavente R. The nuclear lamins. A multigene family of proteins in evolution and differentiation. Exp Cell Res. 1986 Jan;162(1):1–10. doi: 10.1016/0014-4827(86)90421-0. [DOI] [PubMed] [Google Scholar]
  13. Lin H. F., Wolfner M. F. The Drosophila maternal-effect gene fs(1)Ya encodes a cell cycle-dependent nuclear envelope component required for embryonic mitosis. Cell. 1991 Jan 11;64(1):49–62. doi: 10.1016/0092-8674(91)90208-g. [DOI] [PubMed] [Google Scholar]
  14. Lopez J. M., Song K., Hirshfeld A. B., Lin H., Wolfner M. F. The Drosophila fs(1)Ya protein, which is needed for the first mitotic division, is in the nuclear lamina and in the envelopes of cleavage nuclei, pronuclei, and nonmitotic nuclei. Dev Biol. 1994 May;163(1):202–211. doi: 10.1006/dbio.1994.1136. [DOI] [PubMed] [Google Scholar]
  15. Mohler J. D. Developmental genetics of the Drosophila egg. I. Identification of 59 sex-linked cistrons with maternal effects on embryonic development. Genetics. 1977 Feb;85(2):259–272. doi: 10.1093/genetics/85.2.259. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Mount S. M. A catalogue of splice junction sequences. Nucleic Acids Res. 1982 Jan 22;10(2):459–472. doi: 10.1093/nar/10.2.459. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Risau W., Saumweber H., Symmons P. Monoclonal antibodies against a nuclear membrane protein of Drosophila. Localization by indirect immunofluorescence and detection of antigen using a new protein blotting procedure. Exp Cell Res. 1981 May;133(1):47–54. doi: 10.1016/0014-4827(81)90355-4. [DOI] [PubMed] [Google Scholar]
  18. Sharp P. A. Splicing of messenger RNA precursors. Science. 1987 Feb 13;235(4790):766–771. doi: 10.1126/science.3544217. [DOI] [PubMed] [Google Scholar]

Articles from Genetics are provided here courtesy of Oxford University Press

RESOURCES