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Cell
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Cell
Article . 2005
License: Elsevier Non-Commercial
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Cell
Article . 2005 . Peer-reviewed
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Cell
Article . 2006
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Identification of Two Proteins Required for Conjunction and Regular Segregation of Achiasmate Homologs in Drosophila Male Meiosis

Authors: Thomas, Sharon E.; Soltani-Bejnood, Morvarid; Roth, Peggy; Dorn, Rainer; Logsdon, John M.; McKee, Bruce D.;

Identification of Two Proteins Required for Conjunction and Regular Segregation of Achiasmate Homologs in Drosophila Male Meiosis

Abstract

In Drosophila males, homologous chromosomes segregate by an unusual process involving physical connections not dependent on recombination. We have identified two meiotic proteins specifically required for this process. Stromalin in Meiosis (SNM) is a divergent member of the SCC3/SA/STAG family of cohesin proteins, and Modifier of Mdg4 in Meiosis (MNM) is one of many BTB-domain proteins expressed from the mod(mdg4) locus. SNM and MNM colocalize along with a repetitive rDNA sequence known to function as an X-Y pairing site to nucleolar foci during meiotic prophase and to a compact structure associated with the X-Y bivalent during prometaphase I and metaphase I. Additionally, MNM localizes to autosomal foci throughout meiosis I. These proteins are mutually dependent for their colocalization, and at least MNM requires the function of teflon, another meiotic gene. SNM and MNM do not colocalize with SMC1, suggesting that the homolog conjunction mechanism is independent of cohesin.

Keywords

Chromosome Aberrations, Male, Biochemistry, Genetics and Molecular Biology(all), Chromosomal Proteins, Non-Histone, Diptera, Molecular Sequence Data, Cell Cycle Proteins, Exons, DNA, Ribosomal, Chromosomes, Fungal Proteins, Chromosome Pairing, Meiosis, Drosophila melanogaster, Nondisjunction, Genetic, Chromosome Segregation, Mutation, Animals, Drosophila Proteins, Female, Cell Nucleus Division

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
82
Top 10%
Top 10%
Top 10%
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