Natsuume-Sakai S, Nonaka M, Nonaka M, Harada Y, Shreffler D C, Moriwaki K
Department of Immunobiology, Kanazawa University, Japan.
J Immunol. 1990 Jan 1;144(1):358-62.
Three allotypes of murine factor H have been identified serologically in the previous study (denoted H.1, H.2, and H.3). A cDNA clone coding for the entire length of murine factor H was isolated from a library constructed from the livers of STR/N mice which have H.2 allotype and was fully sequenced. The insert of this clone (STR309) contained 4184 nucleotides and consisted of a 47-bp 5' noncoding region, a 54-bp coding for leader peptide, a 3648 bp for the mature factor H protein, and a 435-bp 3' noncoding region. Compared with the previously reported sequence of the cDNA clone (MH8) isolated from B10.WR mice that have H.1 allotype, the size of the protein coding region was exactly the same, but 21 nucleotide substitutions resulting in 15 amino acid replacements were observed. The amino acid replacement/nucleotide substitution ratio (0.71) is far higher than those observed in the allotypic variations of other proteins. Four 15-base oligonucleotide probes specific for either STR309 or MH8 were synthesized and used in Northern blot analysis. The probes specific for STR309 hybridized with mRNA isolated from the livers of STR/N mice but not with mRNA from the livers of BALB/c mice that have H.1 allotype, whereas the reverse pattern was observed with the oligonucleotide probes specific for MH8. These results strongly suggest that the nucleotide sequence of STR309 represents H.2 allotype of factor H protein, providing an example of an unusual allotype with high ratio of amino acid replacements to nucleotide substitutions.
在先前的研究中已通过血清学方法鉴定出三种小鼠补体因子H的同种异型(分别命名为H.1、H.2和H.3)。从具有H.2同种异型的STR/N小鼠肝脏构建的文库中分离出一个编码小鼠补体因子H全长的cDNA克隆,并对其进行了全序列测定。该克隆(STR309)的插入片段包含4184个核苷酸,由一个47bp的5'非编码区、一个编码前导肽的54bp区域、一个编码成熟补体因子H蛋白的3648bp区域以及一个435bp的3'非编码区组成。与先前报道的从具有H.1同种异型的B10.WR小鼠中分离出的cDNA克隆(MH8)序列相比,蛋白质编码区的大小完全相同,但观察到21个核苷酸替换,导致15个氨基酸替换。氨基酸替换/核苷酸替换比率(0.71)远高于在其他蛋白质同种异型变异中观察到的比率。合成了四种分别对STR309或MH8特异的15碱基寡核苷酸探针,并用于Northern印迹分析。对STR309特异的探针与从STR/N小鼠肝脏分离的mRNA杂交,但不与具有H.1同种异型的BALB/c小鼠肝脏的mRNA杂交,而对MH8特异的寡核苷酸探针则观察到相反的杂交模式。这些结果强烈表明,STR309的核苷酸序列代表补体因子H蛋白的H.2同种异型,提供了一个氨基酸替换与核苷酸替换比率高的不寻常同种异型的例子。