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一个连接人类X染色体短臂上类固醇硫酸酯酶基因座和卡尔曼综合征基因座的酵母人工染色体重叠群。

A yeast artificial chromosome contig linking the steroid sulfatase and Kallmann syndrome loci on the human X chromosome short arm.

作者信息

Lee W C, Ferrero G B, Chinault A C, Yen P H, Ballabio A

机构信息

Division of Medical Genetics, Harbor-UCLA Medical Center, Torrance 90502.

出版信息

Genomics. 1993 Oct;18(1):1-6. doi: 10.1006/geno.1993.1419.

Abstract

In this report we describe the construction of a yeast artificial chromosome (YAC) contig linking the steroid sulfatase (STS) and Kallmann syndrome (KAL) loci on Xp22.3. Four human YAC libraries were screened initially with sequences from DXS237 (GMGX9), DXS278 (S232B), and KAL and later with primers from exon 10 of the STS gene and the end fragment of a YAC clone YGX3 to fill the gaps. Fifteen clones were isolated and the sizes of their human inserts were determined by pulsed-field gel electrophoresis followed by Southern hybridization with labeled total human DNA. Overlaps between the YAC clones were evaluated using more than 20 DNA markers, including the screening probes, the end fragments, and the Alu-PCR products of the YAC clones. The extent of overlapping between the clones was further determined by long-range restriction mapping. In combination with our previously reported YAC contigs around STS and KAL, a total of 2 Mb of Xp22.3 have been isolated in YAC clones. These clones will facilitate the isolation of new genes and the characterization of deletions and translocations which occur at very high frequency in this region of the human X chromosome.

摘要

在本报告中,我们描述了一个酵母人工染色体(YAC)重叠群的构建,该重叠群连接了位于Xp22.3上的类固醇硫酸酯酶(STS)和卡尔曼综合征(KAL)基因座。最初用DXS237(GMGX9)、DXS278(S232B)和KAL的序列筛选了四个人类YAC文库,随后用STS基因第10外显子的引物和一个YAC克隆YGX3的末端片段来填补缺口。分离出15个克隆,并通过脉冲场凝胶电泳,然后用标记的总人类DNA进行Southern杂交来确定其人类插入片段的大小。使用20多种DNA标记评估YAC克隆之间的重叠情况,包括筛选探针、末端片段和YAC克隆的Alu-PCR产物。通过长距离限制性图谱进一步确定克隆之间的重叠程度。结合我们之前报道的围绕STS和KAL的YAC重叠群,在YAC克隆中总共分离出了2 Mb的Xp22.3。这些克隆将有助于新基因的分离以及对人类X染色体该区域高频发生的缺失和易位的特征分析。

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