Brenner V, Nyakatura G, Rosenthal A, Platzer M
Institut für Molekulare Biotechnologie, Jena, Germany.
Genomics. 1997 Aug 15;44(1):8-14. doi: 10.1006/geno.1997.4822.
In this paper we present the entire genomic sequence as well as the cDNA sequence of two new human genes encoding the gamma subunit of the NAD(+)-dependent isocitrate dehydrogenase (H-IDH gamma) and the translocon-associated protein delta subunit (TRAP delta). These genes are located on region q28 of the human X chromosome, approximately 70 kb telomeric to the adrenoleukodystrophy locus (ALD). The sequences of the transcripts of both genes were obtained by searching the EST database with genomic data. Identified ESTs were completely sequenced and assembled to cDNAs comprising the entire coding region. For IDH gamma, several EST clones indicate differential splicing. IDH gamma and TRAP delta are arranged in a compact head to head manner. The nontranscribed intergenic region represents only 133 bp and is embedded in a CpG island. The CpG island obviously functions as a bidirectional promoter to initiate the transcription of both functionally unrelated genes with quite distinct expression patterns. This exceptional gene arrangement prompted us to clone and sequence genomic DNA fragments containing the homologous intergenic regions of rat and mouse. We show that in both species this area is similarly compact and represents less than 249 bp in rat and not more than 164 bp in mouse. In both cases this intergenic region is embedded in a CpG island and is highly conserved with nucleotide identity values ranging from 70.1% between human and rat to 92.6% between mouse and rat.
在本文中,我们展示了两个新的人类基因的完整基因组序列以及cDNA序列,这两个基因分别编码NAD(+)依赖的异柠檬酸脱氢酶的γ亚基(H-IDHγ)和转位子相关蛋白δ亚基(TRAPδ)。这些基因位于人类X染色体的q28区域,距离肾上腺脑白质营养不良基因座(ALD)约70 kb的端粒位置。通过用基因组数据搜索EST数据库获得了这两个基因转录本的序列。对鉴定出的EST进行了完整测序,并组装成包含整个编码区的cDNA。对于IDHγ,几个EST克隆显示存在可变剪接。IDHγ和TRAPδ以紧密的头对头方式排列。非转录的基因间隔区仅为133 bp,且嵌入在一个CpG岛中。该CpG岛显然作为双向启动子,启动了两个功能不相关且具有截然不同表达模式的基因的转录。这种特殊的基因排列促使我们克隆并测序包含大鼠和小鼠同源基因间隔区的基因组DNA片段。我们发现,在这两个物种中,该区域同样紧密,大鼠中该区域小于249 bp,小鼠中不超过164 bp。在这两种情况下,该基因间隔区都嵌入在一个CpG岛中,并且高度保守,人与大鼠之间的核苷酸同一性值为70.1%,小鼠与大鼠之间为92.6%。