Suppr超能文献

ZNF75:KRAB锌指基因亚家族cDNA克隆的分离,该克隆定位于HPRT端粒方向1兆碱基处的酵母人工染色体中。

ZNF75: isolation of a cDNA clone of the KRAB zinc finger gene subfamily mapped in YACs 1 Mb telomeric of HPRT.

作者信息

Villa A, Zucchi I, Pilia G, Strina D, Susani L, Morali F, Patrosso C, Frattini A, Lucchini F, Repetto M

机构信息

Istituto di Tecnologie Biomediche Avanzate, Consiglio Nazionale delle Ricerche, Milan, Italy.

出版信息

Genomics. 1993 Nov;18(2):223-9. doi: 10.1006/geno.1993.1459.

Abstract

We have previously mapped a zinc finger genomic motif (ZNF75) to the Xq26 cytogenetic band by using a hybrid panel. Here, we report the isolation of the transcribed counterpart in a cDNA clone and its further localization. The cDNA clone, from a lung fibroblast library, is assembled from three exons, including a 289 amino acid (AA) long open reading frame containing a recently described motif, the Kruppel-associated box, 42 AA long, in exon 2. By comparison with other reported members of the subfamily, the exon-intron boundaries also appear to be very well conserved. Further analysis allowed us to map this gene 1 Mb downstream from the HPRT gene in the published YAC contig that extends across Xq26. Two other motifs, 87 and 78% homologous to ZNF75 at the amino acid level, were identified by PCR on total human DNA, but map outside Xq24-qter.

摘要

我们之前通过使用杂交细胞系将一个锌指基因组基序(ZNF75)定位到了细胞遗传学带Xq26上。在此,我们报告在一个cDNA克隆中分离出其转录对应物及其进一步定位。该cDNA克隆来自肺成纤维细胞文库,由三个外显子组装而成,包括一个289个氨基酸(AA)长的开放阅读框,在第2外显子中包含一个最近描述的基序,即42个AA长的Kruppel相关框。与该亚家族其他已报道成员相比,外显子 - 内含子边界似乎也非常保守。进一步分析使我们能够在已发表的跨越Xq26的YAC重叠群中将该基因定位在HPRT基因下游1 Mb处。通过对人总DNA进行PCR,鉴定出另外两个在氨基酸水平上与ZNF75分别有87%和78%同源性的基序,但它们定位于Xq24 - qter之外。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验