McKee B D
Department of Biochemistry and Cellular and Molecular Biology, University of Tennessee, Knoxville, TN 37996, USA.
Chromosoma. 1996 Sep;105(3):135-41. doi: 10.1007/BF02509494.
Sites for pairing and segregation of achiasmatic bivalents have been characterized in both male and female meiosis in Drosophila melanogaster. The major sex chromosome pairing site in male meiosis corresponds to the intergenic spacer repeats of the rDNA arrays, which are located in the heterochromatin of the X and Y. The sex chromosome pairing sites in females are also heterochromatic, but involve different repeated sequences. In males, weak pairing sites are widely distributed along euchromatin but not heterochromatin of chromosome 2, an autosome. One strong site for male meiotic pairing has been identified on chromosome 2; it overlaps with the his locus, which contains the repetitive structural genes for the histones. In females the sites for pairing of chromosome 4, another autosome, are restricted to the heterochromatin. Thus for both sex chromosomes and autosomes, sites for achiasmatic pairing are heterochromatic in females but euchromatic (except for the rDNA) in males. The possible roles of sequence repetition and of transcription in chromosome pairing are discussed.
在黑腹果蝇的雄性和雌性减数分裂中,无交叉二价体配对和分离的位点已得到表征。雄性减数分裂中的主要性染色体配对位点对应于rDNA阵列的基因间隔区重复序列,这些序列位于X和Y的异染色质中。雌性的性染色体配对位点也是异染色质的,但涉及不同的重复序列。在雄性中,弱配对位点广泛分布于常染色体2(一条常染色体)的常染色质上,而非异染色质上。在染色体2上已鉴定出一个雄性减数分裂配对的强位点;它与his基因座重叠,该基因座包含组蛋白的重复结构基因。在雌性中,另一条常染色体4的配对位点局限于异染色质。因此,对于性染色体和常染色体而言,无交叉配对位点在雌性中是异染色质的,而在雄性中是常染色质的(rDNA除外)。文中讨论了序列重复和转录在染色体配对中的可能作用。