Suppr超能文献

转发至牛6号染色体的详细序列图谱。

Forward to a detailed sequence map of bovine chromosome 6.

作者信息

Weikard R, Goldammer T, Womack J E, Kuehn C

机构信息

Forschungsinstitut fur die Biologie landwirtschaftlicher Nutztiere (FBN), Dummerstorf, Germany.

出版信息

Cytogenet Genome Res. 2007;116(1-2):72-9. doi: 10.1159/000097420.

Abstract

Numerous QTL for a variety of phenotypic traits in dairy and beef cattle have been mapped on bovine chromosome 6 (BTA6). The complete and validated information on the molecular genome organization is an essential prerequisite for the conclusive identification of the causative sequence variation underlying the QTL. In our study we describe efforts to improve the genomic sequence map assembly of BTA6 by filling-in gaps and by suggesting sequence contig rearrangements. This is achieved by the generation and in silico mapping of BAC-end sequences (BESs) from clones containing sequences placed on our high-resolution radiation hybrid (RH) map of BTA6 onto the genome sequence map. Linking high-resolution RH mapping with in silico mapping of BESs on BTA6 enabled the detection of discrepancies in chromosomal assignments of genome sequence contigs and improved the resolution of non-conclusive assignments on the genome sequence assembly. Furthermore, 37% of BESs enabled chromosomal assignment of contigs previously unassigned. Anchoring of 66% of BESs onto HSA4 confirmed the synteny of the respective region of BTA6 including the known evolutionary breakpoints. The BESs will play an important role in the ongoing efforts to complete the sequence of the bovine genome and will also provide a source for the identification of new polymorphic sites in the genome sequence to resolve QTL-containing intervals.

摘要

许多影响奶牛和肉牛各种表型性状的数量性状基因座(QTL)已定位在牛的6号染色体(BTA6)上。关于分子基因组组织的完整且经过验证的信息,是最终确定QTL潜在致病序列变异的必要前提。在我们的研究中,我们描述了通过填补缺口和建议序列重叠群重排来改进BTA6基因组序列图谱组装的工作。这是通过从包含位于我们的BTA6高分辨率辐射杂种(RH)图谱上的序列的克隆中生成BAC末端序列(BES)并进行电子定位来实现的,即将这些BES定位到基因组序列图谱上。将高分辨率RH图谱与BTA6上BES的电子定位相结合,能够检测基因组序列重叠群在染色体分配上的差异,并提高了基因组序列组装中不确定分配的分辨率。此外,37%的BES能够对以前未分配的重叠群进行染色体定位。66%的BES定位到人类4号染色体(HSA4)上,证实了BTA6相应区域的同线性,包括已知的进化断点。这些BES将在目前完成牛基因组序列的工作中发挥重要作用,也将为识别基因组序列中的新多态性位点提供来源,以解析包含QTL的区间。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验