Sweadner K J, Wetzel R K, Arystarkhova E
Neuroscience Center, Massachusetts General Hospital, 149 13th Street, Charlestown, Massachusetts 02129, USA.
Biochem Biophys Res Commun. 2000 Dec 9;279(1):196-201. doi: 10.1006/bbrc.2000.3907.
Although the gamma subunit of the Na,K-ATPase has only 66 or 68 amino acids, its human gene (FXYD2) was found to span 9.2 kb and have seven exons, including two alternatively spliced exons encoding different N-termini. Two candidate promoters with consensus sites for transcription factors Sp1, AP-1, and AP-2 are present, consistent with independent transcription of the splice variants. Multiple ESTs support the transcriptional competence of the identified gene elements. In the FXYD2 gene, there are two closely spaced polyadenylation signals, and both are used. A proposed third splice variant encoding a 31-residue N-terminal extension was not found in the gene, nor was the predicted larger protein found in human kidney Na,K-ATPase. Instead, evidence was found for the origin of the larger cDNA clone in homologous recombination with unrelated DNA from chromosome 2. FXYD2 is on chromosome 11q23 close to a site of tumorigenic chromosomal translocations, and has a number of repeat elements.
尽管钠钾ATP酶的γ亚基仅有66或68个氨基酸,但其人类基因(FXYD2)跨度为9.2 kb,有7个外显子,包括两个编码不同N端的可变剪接外显子。存在两个具有转录因子Sp1、AP-1和AP-2共有位点的候选启动子,这与剪接变体的独立转录一致。多个EST支持所鉴定基因元件的转录活性。在FXYD2基因中,有两个紧密相邻的聚腺苷酸化信号,二者均被使用。在该基因中未发现编码31个残基N端延伸的第三个剪接变体的证据,在人肾钠钾ATP酶中也未发现预测的更大蛋白质。相反,发现有证据表明更大的cDNA克隆起源于与2号染色体上不相关DNA的同源重组。FXYD2位于11q23染色体上,靠近致瘤性染色体易位位点,并有多个重复元件。