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PMID: 8844151 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Selective loss of sperm bearing a compound chromosome in the Drosophila female.

Genetics ·Vol. 143 ·No. 4 ·1996-08-00 ·Pages 1629-42

Dernburg AF, Daily DR, Yook KJ, Corbin JA, Sedat JW, Sullivan W

Abstract

The Drosophila compound entire second chromosome, C(2)EN, displays paternal transmission well below Mendelian expectations (NOVITSKI et al. 1981). Because C(2)EN stocks also show higher-than-expected rates of zygotic lethality, it was proposed that this reduced paternal inheritance might be wholly or partially due to postfertilization events. Efforts to investigate this phenomenon have been hampered because the progeny of crosses between C(2)EN-bearing individuals and those with normal karyotypes die during embryogenesis. We have circumvented this obstacle by employing fluorescence in situ hybridization to directly karyotype early embryos from crosses involving C(2)EN-bearing individuals. This analysis reveals that the distortion in paternal transmission is established before fertilization. Moreover, measurement of the sperm ratios within both the male and female reproductive organs demonstrates that C(2)EN-bearing sperm are selectively lost after sperm transfer to the female and before storage of sperm in the seminal receptacles and spermathecae. Our results are consistent with a model of meiotic drive in which aberrations occurring early in meiosis lead ultimately to sperm dysfunction.

MeSH Terms
Animals Chromosomes/ultrastructure Crosses, Genetic Drosophila/embryology,genetics,ultrastructure Female In Situ Hybridization, Fluorescence Karyotyping Male Meiosis/genetics Mitosis/genetics Models, Genetic Spermatozoa/physiology,ultrastructure
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Dernburg A F
Department of Biochemistry and Biophysics, University of California, San Francisco 94143-0554, USA.
Daily D R
Yook K J
Corbin J A
Sedat J W
Sullivan W
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Article Info
Journal
Genetics
Abbr.
Genetics
ISSN
0016-6731
Published
1996-08-00
Pages
1629-42
Language
English
Region
United States
NLM ID
0374636
PMCID
PMC1207426
Subset
IM
Grants
NIGMS NIH HHS · GM-25101 · United States
NIGMS NIH HHS · GM-46409 · United States
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