Crossover interference is abolished in the absence of a synaptonemal complex protein
Crossover interference is abolished in the absence of a synaptonemal complex protein
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DOI:
10.1016/0092-8674(94)90197-x
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发表时间:
1994-10
期刊:
影响因子:
64.5
通讯作者:
M. Sym;G. Roeder
中科院分区:
文献类型:
--
作者:
M. Sym;G. Roeder
In the zip7 mutant, meiotic chromosomes fail to synapse, owing to the absence of a structural component of the synaptonemal complex (SC). This mutant has been analyzed for the ability to carry out several functions that have been proposed for the SC. The data presented show that the zip1 mutation does not affect chiasma function and confers only modest defects in meiottc recombination and sister chromatid cohesion. In contrast, crossover interference is completely abolished in the absence of Zipl. These data are the first to establish a molecular link between cytological observations of the SC and the genetic phenomenon of interference. introductionThe synaptonemal complex (SC) is an elaborate macromolecular assembly of proteins found along the lengths of homologous chromosomes during meiosis (von Wettstein et al., 1984). Premeiotic DNA replication is followed by a series of events during prophase I that brings homologous chromosomes together and promotes genetic recombination. In yeast, the earliest detectable intermediates in SC morphogenesis can be seen as short stretches of protein cores called axial elements that form along each pair of sister chromatids (Dresser and Giroux, 1966; Alani et al., 1990). As these cores elongate, intimate associations between homologous axial elements begin to form in the context of SC. Once axial elements are assembled into the SC, they are referred to as lateral elements. The area between two lateral elements is referred to as the central region. During the pachytene stage of prophase I, each pair of homologs is fully synapsed, and the SC appears as a ribbon-like structure along the entire length of each chromosome pair.