Heiss N S, Poustka A
Department of Molecular Genome Analysis, Deutsches Krebsforschungszentrum, Heidelberg, Germany.
Genomics. 1997 Oct 1;45(1):224-8. doi: 10.1006/geno.1997.4922.
A transcript map was previously constructed in the 1200-kb telomeric region of Xq28. One of the cDNAs, XAP121, displayed homology to a p64 bovine chloride channel and to a human chloride channel (p64CLCP, NCC27) at both the nucleotide and the peptide levels. In addition, all three sequences exhibited homologies to numerous ESTs derived from human, mouse, rat and pig. While the human NCC27 and XAP121 homologs encode small peptides of 241 and 243 amino acids, respectively, the bovine peptide has a length of 437 amino acids. This suggests that the human genes represent a novel and separate class of small chloride channels. Unlike other chloride channels, the NCC27 peptide was recently shown to localize intracellularly in the cytoplasm and nucleus. The NCC27 and XAP121 genes have thus been designated CLIC1 and CLIC2 for chloride intracellular channel genes 1 and 2, respectively. Since a direct association exists between a number of human chloride channel genes and a range of hereditary diseases, CLIC2 possibly represents a candidate for one of the many diseases linked to Xq28. To facilitate defined mutation analyses, we determined the genomic structure of the CLIC2 gene.
先前在Xq28的1200 kb端粒区域构建了转录图谱。其中一个cDNA,即XAP121,在核苷酸和肽水平上均与一种p64牛氯通道以及一种人类氯通道(p64CLCP,NCC27)具有同源性。此外,所有这三个序列与源自人类、小鼠、大鼠和猪的众多EST均表现出同源性。虽然人类NCC27和XAP121的同源物分别编码241和243个氨基酸的小肽,但牛肽的长度为437个氨基酸。这表明人类基因代表了一类新型且独立的小氯通道。与其他氯通道不同,最近发现NCC27肽定位于细胞质和细胞核内。因此,NCC27和XAP121基因分别被命名为CLIC1和CLIC2,即细胞内氯通道基因1和2。由于许多人类氯通道基因与一系列遗传性疾病之间存在直接关联,CLIC2可能是与Xq28相关的众多疾病之一的候选基因。为便于进行明确的突变分析,我们确定了CLIC2基因的基因组结构。