Kloek A P, McCarter J P, Setterquist R A, Schedl T, Goldberg D E
Department of Molecular Microbiology, Howard Hughes Medical Institute, Washington University School of Medicine, St. Louis, MO 63110, USA.
J Mol Evol. 1996 Aug;43(2):101-8. doi: 10.1007/BF02337354.
Globin genes from the Caenorhabditis species briggsae and remanei were identified and compared with a previously described C. elegans globin gene. The encoded globins share between 86% and 93% amino acid identity, with most of the changes in or just before the putative B helix. C. remanei was found to have two globin alleles, Crg1-1 and Crg1-2. The coding sequence for each is interrupted by a single intron in the same position. The exons of the two genes are only 1% divergent at the nucleotide level and encode identical polypeptides. In contrast, intron sequence divergence is 16% and numerous insertions and deletions have significantly altered the size and content of both introns. Genetic crosses show that Crg1-1 and Crg1-2 segregate as alleles. Homozygous lines for each allele were constructed and northern analysis confirmed the expression of both alleles. These data reveal an unusual situation wherein two alleles encoding identical proteins have diverged much more rapidly in their introns than the silent sites of their coding sequences, suggesting multiple gene conversion events.
从秀丽隐杆线虫(Caenorhabditis briggsae)和雷氏隐杆线虫(Caenorhabditis remanei)中鉴定出珠蛋白基因,并与先前描述的秀丽隐杆线虫珠蛋白基因进行比较。编码的珠蛋白具有86%至93%的氨基酸同一性,大部分变化发生在假定的B螺旋中或其之前。发现雷氏隐杆线虫有两个珠蛋白等位基因,即Crg1-1和Crg1-2。每个等位基因的编码序列都被同一位置的单个内含子打断。这两个基因的外显子在核苷酸水平上仅有1%的差异,且编码相同的多肽。相比之下,内含子序列差异为16%,大量的插入和缺失显著改变了两个内含子的大小和内容。遗传杂交表明Crg1-1和Crg1-2作为等位基因分离。构建了每个等位基因的纯合系,Northern分析证实了两个等位基因的表达。这些数据揭示了一种不寻常的情况,即编码相同蛋白质的两个等位基因在其内含子中的分歧比其编码序列的沉默位点快得多,这表明发生了多次基因转换事件。