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小鼠8号染色体臂间倒位的分子特征表明端粒是减数分裂重组的启动子。

Molecular characterization of a pericentric inversion in mouse chromosome 8 implicates telomeres as promoters of meiotic recombination.

作者信息

Ashley T, Cacheiro N L, Russell L B, Ward D C

机构信息

Department of Genetics, Yale University School of Medicine, New Haven, CT 06510.

出版信息

Chromosoma. 1993 Jan;102(2):112-20. doi: 10.1007/BF00356028.

Abstract

A "hot spot" of meiotic recombination has been found in males on murine chromosome 8 using nonisotopic hybridization of a series of probes to mitotic and meiotic chromosomes. The sequences responsible for this enhanced recombination are the telomeric repeats. Mice both normal and hetero- or homozygous for a pericentric inversion, In(8)1 Rl, were analyzed. The inversion subdivides chromosome 8 into three discreet regions: (1) a fraction of the micro "short arm" that contains 30-150 kb of telomeric sequences and only about one-fifth of the contiguous minor-satellite sequences (approximately 200 kb); (2) the inverted region; and (3) the noninverted distal two-thirds of the chromosome. In 70 spermatocytes from inversion heterozygotes, examined by electron microscopy, synapsis of the inverted region was complete but entirely nonhomologous. Nonhomologous synapsis persists from initiation of synaptonemal complex formation in zygonema/early pachynema until dissolution in late pachynema. This nonhomologous synapsis also suppresses crossing over within the inverted segment. The opportunity for proximal homologous recombination is thus restricted to the roughly 250 kb segment located between the short-arm break and the end of the bivalent. Nonetheless, an extreme proximal chiasma was observed in 11% of the heterozygous chromosome-8 bivalents, 34% of the normal 8 bivalents and 35% of the homozygous inversion 8 bivalents from spermatocyte preparations. Since in the normal chromosomes all minor satellite sequences are adjacent to the telomere, while in the inversion chromosomes most of these sequences are transposed to an interstitial position without a corresponding shift in chiasma position, the minor-satellite sequences can be ruled out as promoters of recombination.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

利用一系列探针与有丝分裂和减数分裂染色体的非同位素杂交技术,在雄性小鼠的8号染色体上发现了一个减数分裂重组的“热点”。导致这种重组增强的序列是端粒重复序列。对正常以及因着丝粒周围倒位In(8)1 Rl而产生的杂合或纯合小鼠进行了分析。该倒位将8号染色体分为三个离散区域:(1) 一小部分微小“短臂”,包含30 - 150 kb的端粒序列,仅约五分之一的连续小卫星序列(约200 kb);(2) 倒位区域;(3) 染色体未倒位的远端三分之二部分。通过电子显微镜检查70个倒位杂合子的精母细胞,发现倒位区域的联会是完整的,但完全是非同源的。从偶线期/早粗线期联会复合体形成开始到粗线期末解体,非同源联会一直持续。这种非同源联会也抑制了倒位片段内的交叉互换。因此,近端同源重组的机会仅限于位于短臂断裂点和二价体末端之间约250 kb的片段。然而,在精母细胞制备物中,11%的杂合8号染色体二价体、34%的正常8号染色体二价体和35%的纯合倒位8号染色体二价体中观察到了极端近端交叉。由于在正常染色体中所有小卫星序列都与端粒相邻,而在倒位染色体中,这些序列中的大多数被转移到了中间位置,交叉位置没有相应变化,因此可以排除小卫星序列作为重组促进因子的可能性。(摘要截短于250词)

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