Doak T G, Witherspoon D J, Doerder F P, Williams K, Herrick G
Department of Oncological Science, University of Utah, Salt Lake City 84132, USA.
Genetica. 1997;101(2):75-86. doi: 10.1023/a:1018331118647.
The complete sequences of four TBE1 transposons from Oxytricha fallax and O. trifallax are presented and analyzed. Although two TBE1s are 98% identical to each other at the nucleotide level, the remaining two TBE1s are only 90% identical both to each other and to the other two. This large evolutionary divergence allows us to identify conserved TBE1 features. TBE1 transposons are 4.1 kbp long and are flanked by 3 bp target-site repeats. The elements consist of 78 bp inverted terminal repeats, of which the 17 terminal base pairs are Oxytricha telomere repeats; a central conserved section of 550 bp that includes a set of nested direct and inverted sequence repeats; and 3 open reading frames conserved for encoded amino acid sequence. The three open reading frames encode a 22 kDa basic protein of unknown function, a 42 kDa 'D,D35E' transposase, and a 57 kDa chimeric C2H2 zinc finger/protein kinase. The protein kinase domain of the 57 kDa protein is unusual, lacking a conserved ATP-binding motif.
本文展示并分析了来自草履虫(Oxytricha fallax)和三刺草履虫(O. trifallax)的四个TBE1转座子的完整序列。尽管其中两个TBE1在核苷酸水平上彼此有98%的同一性,但其余两个TBE1彼此之间以及与另外两个TBE1的同一性仅为90%。这种较大的进化差异使我们能够识别保守的TBE1特征。TBE1转座子长度为4.1千碱基对(kbp),两侧是3个碱基对的靶位点重复序列。这些元件由78个碱基对的反向末端重复序列组成,其中17个末端碱基对是草履虫端粒重复序列;一个550碱基对的中央保守区域,包括一组嵌套的正向和反向序列重复;以及3个在编码氨基酸序列上保守的开放阅读框。这三个开放阅读框分别编码一个功能未知的22千道尔顿碱性蛋白、一个42千道尔顿的“D,D35E”转座酶和一个57千道尔顿的嵌合C2H2锌指/蛋白激酶。57千道尔顿蛋白的蛋白激酶结构域不同寻常,缺乏保守的ATP结合基序。