Ponte I, Monsalves C, Cabañas M, Martínez P, Suau P
Departamento de Bioquímica i Biología Molecular, Facultad de Ciencias, Universidad Autónoma de Barcelona, Barcelona, Spain.
J Mol Evol. 1996 Aug;43(2):125-34. doi: 10.1007/BF02337357.
The H10 gene has a long 3' untranslated region (3'UTR) of 1,125 nucleotides in the rat and 1,310 in humans. Analysis of the sequences shows that they have features of simple DNA that suggest involvement of replication slippage in their evolution. These features include the length imbalance between the rat and human sequences; the abundance of single-base repeats, two-base runs and other simple motifs clustered along the sequence; and the presence of single-base repeat length polymorphisms in the rat and mouse sequences. Pairwise comparisons show numerous short insertions/deletions, often flanked by direct repeats. In addition, a proportion of short insertions/deletions results from length differences in conserved single-base repeats. Quantification of the sequence simplicity shows that simple sequences have been more actively incorporated in the human lineage than in the rodent lineage. The combination of insertions/deletions and nucleotide substitutions along the sequence gives rise to three main regions of homology: a highly variable central region flanked by more conserved regions nearest the coding region and the polyA addition site.
H10基因在大鼠中具有一个长度为1125个核苷酸的长3'非翻译区(3'UTR),在人类中则为1310个核苷酸。对这些序列的分析表明,它们具有简单DNA的特征,这表明复制滑动参与了它们的进化。这些特征包括大鼠和人类序列之间的长度不平衡;沿着序列聚集的单碱基重复、双碱基序列和其他简单基序的丰富性;以及大鼠和小鼠序列中存在单碱基重复长度多态性。成对比较显示出大量的短插入/缺失,其两侧通常为直接重复序列。此外,一部分短插入/缺失是由保守单碱基重复序列的长度差异导致的。序列简单性的量化表明,简单序列在人类谱系中比在啮齿动物谱系中更活跃地被整合。沿着序列的插入/缺失和核苷酸替换的组合产生了三个主要的同源区域:一个高度可变的中央区域,两侧是最靠近编码区和多聚腺苷酸加尾位点的更保守区域。