Analysis of close stable homolog juxtaposition during meiosis in mutants of Saccharomyces cerevisiae.

Abstract:

:A unique aspect of meiosis is the segregation of homologous chromosomes at the meiosis I division. The pairing of homologous chromosomes is a critical aspect of meiotic prophase I that aids proper disjunction at anaphase I. We have used a site-specific recombination assay in Saccharomyces cerevisiae to examine allelic interaction levels during meiosis in a series of mutants defective in recombination, chromatin structure, or intracellular movement. Red1, a component of the chromosome axis, and Mnd1, a chromosome-binding protein that facilitates interhomolog interaction, are critical for achieving high levels of allelic interaction. Homologous recombination factors (Sae2, Rdh54, Rad54, Rad55, Rad51, Sgs1) aid in varying degrees in promoting allelic interactions, while the Srs2 helicase appears to play no appreciable role. Ris1 (a SWI2/SNF2 related protein) and Dot1 (a histone methyltransferase) appear to play minor roles. Surprisingly, factors involved in microtubule-mediated intracellular movement (Tub3, Dhc1, and Mlp2) appear to play no appreciable role in homolog juxtaposition, unlike their counterparts in fission yeast. Taken together, these results support the notion that meiotic recombination plays a major role in the high levels of homolog interaction observed during budding yeast meiosis.

journal_name

Genetics

journal_title

Genetics

authors

Lui DY,Peoples-Holst TL,Mell JC,Wu HY,Dean EW,Burgess SM

doi

10.1534/genetics.105.050658

subject

Has Abstract

pub_date

2006-07-01 00:00:00

pages

1207-22

issue

3

eissn

0016-6731

issn

1943-2631

pii

genetics.105.050658

journal_volume

173

pub_type

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