Muramatsu T, Kincaid R L
Section on Immunology, Laboratory of Molecular and Cellular Neurobiology, National Institute on Alcohol Abuse and Alcoholism, Rockville, MD 20852.
Biochem Biophys Res Commun. 1992 Oct 15;188(1):265-71. doi: 10.1016/0006-291x(92)92379-c.
A cDNA for an alternatively spliced variant of the testis-specific catalytic subunit of calmodulin dependent protein phosphatase (CaM-PrP) was cloned from a human testis library. The nucleotide sequence of 2134 base pairs (bp) encodes a protein of 502 amino acids (Mr approximately 57,132) and pI 7.0. The cDNA sequence differs from the murine form of this gene by a 30 bp deletion in the coding region, the position of which matches those in the two other genes for the catalytic subunit. These data indicate that this alternative splicing event arose prior to the divergence of the three genes. The deduced sequence of the human protein is only 88% identical to the homologous murine form, in striking contrast to the other two CaM-PrP catalytic subunits which are highly conserved between mouse and human (approximately 99%); this indicates a more rapid rate of evolution for the testis-specific gene. Analysis of Southern blots containing DNA from human-hamster somatic cell hybrids show that the gene is on human chromosome 8.
从人睾丸文库中克隆出钙调蛋白依赖性蛋白磷酸酶(CaM-PrP)睾丸特异性催化亚基可变剪接变体的cDNA。2134个碱基对(bp)的核苷酸序列编码一个由502个氨基酸组成的蛋白质(分子量约为57,132),等电点为7.0。该cDNA序列与该基因的鼠类形式在编码区有一个30 bp的缺失,其位置与另外两个催化亚基基因中的位置相匹配。这些数据表明,这种可变剪接事件发生在这三个基因分化之前。推导的人类蛋白质序列与同源鼠类形式的序列只有88%的同一性,这与另外两个在小鼠和人类之间高度保守(约99%)的CaM-PrP催化亚基形成鲜明对比;这表明睾丸特异性基因的进化速度更快。对包含人-仓鼠体细胞杂种DNA的Southern杂交分析表明,该基因位于人类8号染色体上。