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首页> 外文期刊>Journal of Genetics >Expression and identification of folate-sensitive fragile sites in British Suffolk sheep (Ovis aries)
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Expression and identification of folate-sensitive fragile sites in British Suffolk sheep (Ovis aries)

机译:叶酸敏感脆弱位点在英国萨福克绵羊(Ovis aries)中的表达和鉴定

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摘要

An investigation to understand the dynamics and biological significance of fragile site expression, and identification of 5-fluorodeoxyuridine (FUdR) induced chromosomal gaps/breaks, were carried out in an experimental flock of 45 Suffolk sheep. The statistical comparison revealed, highly significant variation in the frequency of chromosomal fragile site expression between control and FUdR cultures. Mean (± S.D.) values for cells with gaps and breaks, or aberrant cell count (AC), and the number of aberrations (NoA) per animal were 2.02 ± 0.34, 2.42 ± 0.48, 13.26 ± 0.85 and 21.87 ± 1.88 (P < 0.01) in control and FUdR cultures, respectively. The comparison of age revealed nonsignificant variation between control and FUdR cultures. The G-band analysis of fragile site data revealed gaps in 29 autosomal and two X-chromosomal bands in the control cultures, whereas FUdR treated cultures scored 78 unstable bands in autosomes of which 56 were significantly fragile. X-chromosomes expressed breaks and gaps in six G-negative bands and five of them (Xq13, Xq15, Xq17, Xq24 and Xq26) were significantly fragile. The distribution comparison of autosomal fragile sites between sex groups did not reveal any significant variation. Female X-chromosomes were significantly more fragile than the male X-chromosomes. The distribution comparison for age groups (lambs versus adults) revealed significantly higher number of fragile bands in adults. Comparison of published data on reciprocal translocations in sheep with the fragile-site data obtained in this study indicated that the break sites of both phenomena were correlated. Similarities were also found between fragile sites and breakpoints of evolutionary significance in family Bovidae.
机译:在45只萨福克绵羊的实验羊群中进行了一项调查,以了解脆弱位点表达的动力学和生物学意义,并鉴定5-氟脱氧尿苷(FUdR)诱导的染色体缺口/断裂。统计比较表明,对照和FUdR培养物之间的染色体易碎位点表达频率有非常显着的变化。具有缺口和断裂或异常细胞计数(AC)的细胞的平均(±SD)值以及每只动物的畸变数(NoA)为2.02±0.34、2.42±0.48、13.26±0.85和21.87±1.88(P < 0.01)分别在对照和FUdR培养物中。年龄比较显示对照和FUdR培养物之间无显着差异。对易碎位点数据的G带分析显示,在对照培养物中29条常染色体和2条X染色体条带中存在缺口,而FUdR处理的培养物在常染色体中划出78条不稳定带,其中56条明显易碎。 X染色体在六个G负条带中表达了断裂和缺口,其中五个(Xq13,Xq15,Xq17,Xq24和Xq26)非常脆弱。性别组间常染色体易碎位点的分布比较未显示任何显着差异。女性X染色体比男性X染色体更脆弱。年龄组(羔羊与成年人)的分布比较显示成年人中易碎带的数量明显增加。将已发表的关于绵羊相互易位的数据与本研究中获得的脆弱位点数据进行比较表明,两种现象的断​​裂位点是相关的。还发现脆弱部位和牛科家族进化重要性断点之间存在相似性。

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