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转录的人类X染色体DNA序列的鉴定与分离

Identification and isolation of transcribed human X chromosome DNA sequences.

作者信息

Kunkel L M, Tantravahi U, Kurnit D M, Eisenhard M, Bruns G P, Latt S A

出版信息

Nucleic Acids Res. 1983 Nov 25;11(22):7961-79. doi: 10.1093/nar/11.22.7961.

Abstract

A human X chromosome specific phage library has been used as a source of X-specific genomic DNA clones which hybridize with cellular RNA. Random cDNA clones were mapped for X chromosome sequence localization and 8 were identified as hybridizing to X chromosome Hind III fragments. All eight also hybridized with autosomal Hind III fragments. The X chromosome genomic sequences corresponding to two of these cDNA clones were isolated from a phage library constructed with the Hind III endonuclease digest products of X enriched DNA. One genomic DNA segment, localized to the short area of the X, shared sequence homology with at least one region of the human Y chromosome. The methodology developed represents a rapid means to obtain a specific genomic DNA clone from a single chromosome when multiple different genomic loci homologous to an expressed DNA sequence exist.

摘要

一个人类X染色体特异性噬菌体文库已被用作与细胞RNA杂交的X特异性基因组DNA克隆的来源。随机cDNA克隆被定位用于X染色体序列定位,其中8个被鉴定为与X染色体Hind III片段杂交。所有这8个克隆也与常染色体Hind III片段杂交。与其中两个cDNA克隆相对应的X染色体基因组序列是从用富含X的DNA的Hind III核酸内切酶消化产物构建的噬菌体文库中分离出来的。一个定位在X染色体短区域的基因组DNA片段与人类Y染色体的至少一个区域具有序列同源性。所开发的方法代表了一种在存在与表达的DNA序列同源的多个不同基因组位点时,从单条染色体快速获得特定基因组DNA克隆的手段。

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