首页> 美国卫生研究院文献>Genome Research >Fine Mapping Suggests that the Goat Polled Intersex Syndrome and the Human Blepharophimosis Ptosis Epicanthus Syndrome Map to a 100-kb Homologous Region
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Fine Mapping Suggests that the Goat Polled Intersex Syndrome and the Human Blepharophimosis Ptosis Epicanthus Syndrome Map to a 100-kb Homologous Region

机译:精细定位表明山羊轮询的双性恋综合征和人类嗜血性支原体眼睑下垂综合征可映射到100-kb同源区域

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摘要

To clone the goat Polled Intersex Syndrome (PIS) gene(s), a chromosome walk was performed from six entry points at 1q43. This enabled 91 BACs to be recovered from a recently constructed goat BAC library. Six BAC contigs of goat chromosome 1q43 (ICC1–ICC6) were thus constructed covering altogether 4.5 Mb. A total of 37 microsatellite sequences were isolated from this 4.5-Mb region (16 in this study), of which 33 were genotyped and mapped. ICC3 (1500 kb) was shown by genetic analysis to encompass the PIS locus in a ∼400-kb interval without recombinants detected in the resource families (293 informative meioses). A strong linkage disequilibrium was detected among unrelated animals with the two central markers of the region, suggesting a probable location for PIS in ∼100 kb. High-resolution comparative mapping with human data shows that this DNA segment is the homolog of the human region associated with Blepharophimosis Ptosis Epicanthus inversus Syndrome (BPES) gene located in 3q23. This finding suggests that homologous gene(s) could be responsible for the pathologies observed in humans and goats.[The sequence data, PCR primers and PCR conditions for STS and microsatellites described in this paper have been submitted to the GenBank data library under accession nos. –, –, –793931, –, –, and –.]
机译:为了克隆山羊Polled Intersex综合征(PIS)基因,从1q43处的六个入口点进行了染色体遍历。这使91个BAC可以从最近构建的山羊BAC库中恢复。这样就构建了六个山羊染色体1q43(ICC1-ICC6)的BAC重叠群,总共覆盖4.5 Mb。从这个4.5 Mb的区域中共分离出37个微卫星序列(本研究中为16个),其中33个已被基因分型并作图。遗传分析表明,ICC3(1500 kb)涵盖了〜400 kb区间的PIS基因座,而在资源家族中未检测到重组体(293个信息灵巧的媒介)。在不相关的动物中,该区域的两个中心标记物之间检测到强烈的连锁不平衡,表明PIS的可能位置约为100 kb。用人类数据进行的高分辨率比较作图表明,该DNA片段是与位于3q23的支气管上睑下垂逆病综合征(BPES)基因相关的人类区域的同源物。这一发现表明同源基因可能是人类和山羊中观察到的病理的原因。[本文描述的STS和微卫星的序列数据,PCR引物和PCR条件已提交给GenBank数据库,登录号为。 –,–,–793931,–,–和–。]

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