Soldatov N M
Laboratory of Cell Biology, Howard Hughes Medical Institute, Rockefeller University, New York, NY 10021-6399.
Proc Natl Acad Sci U S A. 1992 May 15;89(10):4628-32. doi: 10.1073/pnas.89.10.4628.
The nucleotide sequence of cDNA encoding the human fibroblast Ca2+ channel of L type (HFCC) has been determined. It is highly homologous to L-type channels previously cloned from rabbit lung and heart as well as from rat brain. At least four sites of molecular diversity were identified in the nucleotide sequence of HFCC. Three of these include regions encoding the transmembrane segments IIS6, IIIS2, and IVS3, which are known to be important for channel gating properties. The positions of these sites correlate with RNA splice sites, indicating that the molecular diversity of the transcripts is a result of alternative splicing. The fourth diversity region is located at the C-terminal region and comprises insertions and deletions. It is suggested that these variations may give rise to multiple subforms of HFCC with altered electrophysiological properties.
编码人L型成纤维细胞钙通道(HFCC)的cDNA核苷酸序列已被确定。它与先前从兔肺、心脏以及大鼠脑中克隆的L型通道高度同源。在HFCC的核苷酸序列中至少鉴定出四个分子多样性位点。其中三个位点包括编码跨膜片段IIS6、IIIS2和IVS3的区域,已知这些区域对通道门控特性很重要。这些位点的位置与RNA剪接位点相关,表明转录本的分子多样性是可变剪接的结果。第四个多样性区域位于C末端区域,由插入和缺失组成。有人提出,这些变异可能会产生具有改变的电生理特性的HFCC多种亚型。