Ellis N A, Groden J, Ye T Z, Straughen J, Lennon D J, Ciocci S, Proytcheva M, German J
Laboratory of Human Genetics, New York Blood Center, New York 10021, USA.
Cell. 1995 Nov 17;83(4):655-66. doi: 10.1016/0092-8674(95)90105-1.
The Bloom's syndrome (BS) gene, BLM, plays an important role in the maintenance of genomic stability in somatic cells. A candidate for BLM was identified by direct selection of a cDNA derived from a 250 kb segment of the genome to which BLM had been assigned by somatic crossover point mapping. In this novel mapping method, cells were used from persons with BS that had undergone intragenic recombination within BLM. cDNA analysis of the candidate gene identified a 4437 bp cDNA that encodes a 1417 amino acid peptide with homology to the RecQ helicases, a subfamily of DExH box-containing DNA and RNA helicases. The presence of chain-terminating mutations in the candidate gene in persons with BS proved that it was BLM.
布卢姆综合征(BS)基因BLM在维持体细胞基因组稳定性方面发挥着重要作用。通过直接筛选源自基因组250 kb片段的cDNA来鉴定BLM的候选基因,该基因组片段已通过体细胞交叉点定位法确定与BLM相关。在这种新颖的定位方法中,使用了来自患有BS且在BLM基因内发生基因内重组的个体的细胞。对候选基因的cDNA分析鉴定出一个4437 bp的cDNA,其编码一个1417个氨基酸的肽,该肽与RecQ解旋酶具有同源性,RecQ解旋酶是含DExH盒的DNA和RNA解旋酶的一个亚家族。患有BS的个体中候选基因存在链终止突变,这证明它就是BLM。