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通过染色体显带和荧光原位杂交(FISH)绘图技术揭示,牛的罗伯逊易位(1;29)起源于复杂的染色体重排。

Cattle rob(1;29) originating from complex chromosome rearrangements as revealed by both banding and FISH-mapping techniques.

作者信息

Di Meo G P, Perucatti A, Chaves R, Adega F, De Lorenzi L, Molteni L, De Giovanni A, Incarnato D, Guedes-Pinto H, Eggen A, Iannuzzi L

机构信息

National Research Council CNR, ISPAAM, CNR-ISPAAM, Laboratory of Animal Cytogenetics and Gene Mapping, Via Argine 1085, 80147 Naples, Italy.

出版信息

Chromosome Res. 2006;14(6):649-55. doi: 10.1007/s10577-006-1074-1. Epub 2006 Sep 14.

Abstract

Sixteen carriers of rob(1;29) (one of which was homozygous) from six different breeds (four Italian and two Portuguese), two heterozygous carriers of rob(26;29), three river buffaloes and two sheep were cytogenetically investigated in this study by using banding and FISH-mapping techniques (the latter only in cattle and river buffalo). Single- and dual- colour FISH were used with bovine probes containing both INRA143 (mapping proximally to BTA29) and bovine satellite (SAT) DNA SAT I, SAT III and SAT IV (mapping at the centromeric regions of cattle chromosomes). The combined use of these probes, the comparison of rob(1;29) with the dicentric rob(26;29) and with both river buffalo and sheep chromosomes (biarmed pairs) allowed us to hypothezise that rob(1;29) originated from complex chromosomal rearrangements through at least three sequential events: (a) centric fusion with the formation of a dicentric chromosome; (b) formation of a monocentric chromosome with loss of SAT I from both BTA1 and BTA29, most of SAT IV from BTA29 and, probably, some repeats of SAT III from BTA1; (c) double pericentric inversion or, more probably, a chromosome transposition of a small chromosome segment containing INRA143 from proximal p-arms to proximal q-arm of the translocated chromosome.

摘要

本研究采用显带和荧光原位杂交(FISH)映射技术(后者仅用于牛和水牛),对来自六个不同品种(四个意大利品种和两个葡萄牙品种)的16只rob(1;29)携带者(其中一只为纯合子)、2只rob(26;29)杂合携带者、3头河水牛和2只绵羊进行了细胞遗传学研究。使用含有INRA143(定位于BTA29近端)和牛卫星(SAT)DNA SAT I、SAT III和SAT IV(定位于牛染色体着丝粒区域)的牛探针进行单色和双色FISH。这些探针的联合使用、rob(1;29)与双着丝粒rob(26;29)以及与河水牛和绵羊染色体(双臂对)的比较,使我们能够假设rob(1;29)起源于至少三个连续事件导致的复杂染色体重排:(a)通过形成双着丝粒染色体进行着丝粒融合;(b)形成单着丝粒染色体,同时从BTA1和BTA29丢失SAT I,从BTA29丢失大部分SAT IV,并且可能从BTA1丢失一些SAT III重复序列;(c)双着丝粒倒位,或者更有可能是一个包含INRA143的小染色体片段从易位染色体的近端p臂到近端q臂的染色体转位。

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