Peter B, Man Y M, Begg C E, Gall I, Leader D P
Department of Biochemistry, University of Glasgow, Scotland, U.K.
J Mol Biol. 1988 Oct 5;203(3):665-75. doi: 10.1016/0022-2836(88)90200-8.
The nucleotide sequence corresponding to almost the whole of a mouse gamma-cytoskeletal actin mRNA was determined from overlapping cloned DNA copies derived from brain mRNA. Several gamma-actin processed pseudogenes were isolated from a library of cloned DBA mouse genomic DNA, and the nucleotide sequences of these were determined and compared with that of the cDNA. This showed that two of these pseudogenes had arisen from a gene duplication or amplification event, and indicated that they had subsequently undergone partial correction against one another. The relative ages of the pseudogenes were estimated on the basis of their percentage divergence from the cDNA sequence and these were compared with an estimation based on the number of presumed silent mutations in the cDNA since each pseudogene had arisen. Consistent results were obtained, except in the case of one pseudogene which also showed an anomalous regional distribution of differences from the cDNA sequence. One way of accounting for the features of this anomalous pseudogene is by postulating that it is derived from a second functional gene for gamma-actin, different from that represented by the cDNA described here.
从小鼠脑mRNA来源的重叠克隆DNA拷贝中确定了几乎对应于整个小鼠γ-细胞骨架肌动蛋白mRNA的核苷酸序列。从克隆的DBA小鼠基因组DNA文库中分离出几个γ-肌动蛋白加工假基因,并测定了它们的核苷酸序列,并与cDNA的序列进行比较。结果表明,其中两个假基因源于基因复制或扩增事件,并表明它们随后相互进行了部分校正。根据假基因与cDNA序列的差异百分比估计了假基因的相对年龄,并将其与基于每个假基因出现后cDNA中假定沉默突变数量的估计值进行比较。除了一个假基因的情况外,得到了一致的结果,该假基因与cDNA序列的差异也显示出异常的区域分布。解释这个异常假基因特征的一种方法是假设它来自γ-肌动蛋白的第二个功能基因,与这里描述的cDNA所代表的基因不同。