Albig W, Kioschis P, Poustka A, Meergans K, Doenecke D
Institut für Biochemie und Molekulare Zellbiologie, Universität Göttingen, Germany.
Genomics. 1997 Mar 1;40(2):314-22. doi: 10.1006/geno.1996.4592.
We have previously located the genes of the five human main type H1 genes and the gene encoding the testicular subtype H1t to the region 21.1 to 22.2 on the short arm of chromosome 6. To investigate the organization of the histone genes in this region, we isolated two YACs from a human YAC library by PCR screening with primers specific for histone H1.1. This screen revealed two YAC clones, YAC Y23 (corresponding to ICRFy901D1223) contains an insert of about 480 kb, whereas the smaller YAC 4A (corresponding to ICRFy900C104) spans about 340 kb and is completely covered by YAC Y23. We have subcloned the YAC inserts in cosmids, determined the linear orientation of the cosmids by cosmid walking, and constructed a restriction map of the entire region by mapping the individual cosmids using partial digests and hybridization with labeled oligonucleotides complementary to the cos site of the vector. Hybridization analysis, subcloning, restriction mapping, and sequencing revealed that most of the previously isolated phage and cosmid clones containing histone genes are part of this YAC including the clones containing the four human main type H1 histone genes H1.1 to H1.4, the H1t gene, and core histone genes. Thirty-five histone genes map within 260 kb of the YAC Y23 insert. All newly identified histone genes were sequenced, and the sequences were deposited with the EMBL nucleotide sequence database. The histone H1.5 gene is not part of this region, and we therefore conclude that the H1.5 gene and the associated core histone genes form a separate subcluster within this chromosomal region.
我们先前已将人类五种主要类型H1基因以及编码睾丸亚型H1t的基因定位到6号染色体短臂上21.1至22.2区域。为了研究该区域组蛋白基因的组织情况,我们通过用组蛋白H1.1特异性引物进行PCR筛选,从人类YAC文库中分离出两个YAC。该筛选揭示了两个YAC克隆,YAC Y23(对应于ICRFy901D1223)包含约480 kb的插入片段,而较小的YAC 4A(对应于ICRFy900C104)跨度约340 kb,并且完全被YAC Y23覆盖。我们已将YAC插入片段亚克隆到黏粒中,通过黏粒步移确定黏粒的线性方向,并通过使用部分酶切和与与载体cos位点互补的标记寡核苷酸杂交来绘制各个黏粒,从而构建了整个区域的限制性图谱。杂交分析、亚克隆、限制性图谱绘制和测序表明,大多数先前分离的含有组蛋白基因的噬菌体和黏粒克隆都是该YAC的一部分,包括含有四个人类主要类型H1组蛋白基因H1.1至H1.4、H1t基因和核心组蛋白基因的克隆。35个组蛋白基因定位于YAC Y23插入片段的260 kb范围内。所有新鉴定的组蛋白基因都进行了测序,其序列已存入EMBL核苷酸序列数据库。组蛋白H1.5基因不是该区域的一部分,因此我们得出结论,H{1.5}基因和相关的核心组蛋白基因在该染色体区域内形成一个单独的亚簇。