Besansky N J, Paskewitz S M, Hamm D M, Collins F H
Division of Parasitic Diseases, Centers for Disease Control, Atlanta, Georgia 30333.
Mol Cell Biol. 1992 Nov;12(11):5102-10. doi: 10.1128/mcb.12.11.5102-5110.1992.
Two distinct site-specific retrotransposon families, named RT1 and RT2, from the sibling mosquito species Anopheles gambiae and A. arabiensis, respectively, were previously identified. Both were shown to occupy identical nucleotide positions in the 28S rRNA gene and to be flanked by identical 17-bp target site duplications. Full-length representatives of each have been isolated from a single species, A. gambiae, and the nucleotide sequences have been analyzed. Beyond insertion specificity, RT1 and RT2 share several structural and sequence features which show them to be members of the LINE-like, or non-long-terminal-repeat retrotransposon, class of reverse transcriptase-encoding mobile elements. These features include two long overlapping open reading frames (ORFs), poly(A) tails, the absence of long terminal repeats, and heterogeneous 5' truncation of most copies. The first ORF of both elements, particularly ORF1 of RT1, is glutamine rich and contains long tracts of polyglutamine reminiscent of the opa repeat. Near the carboxy ends, three cysteine-histidine motifs occur in ORF1 and one occurs in ORF2. In addition, each ORF2 contains a region of sequence similarity to reverse transcriptases and integrases. Alignments of the protein sequences from RT1 and RT2 reveal 36% identity over the length of ORF1 and 60% identity over the length of ORF2, but the elements cannot be aligned in the 5' and 3' noncoding regions. Unlike that of RT2, the 5' noncoding region of RT1 contains 3.5 copies of a 500-bp subrepeat, followed by a poly(T) tract and two imperfect 55-bp subrepeats, the second spanning the beginning of ORF1. The pattern of distribution of these elements among five siblings species in the A. gambiae complex is nonuniform. RT1 is present in laboratory and wild A. gambiae, A. arabiensis, and A. melas but has not been detected in A. quadriannulatus or A. merus. RT2 has been detected in all available members of the A. gambiae complex except A. merus. Copy number fluctuates, even among the offspring of individual wild female A. gambiae mosquitoes. These findings reflect a complex evolutionary history balancing gain and loss of copies against the coexistence of two elements competing for a conserved target site in the same species for perhaps millions of years.
先前已分别从亲缘关系相近的冈比亚按蚊和阿拉伯按蚊这两种蚊子中鉴定出两个不同的位点特异性逆转座子家族,分别命名为RT1和RT2。二者在28S rRNA基因中占据相同的核苷酸位置,且两侧均有相同的17个碱基对的靶位点重复序列。每个家族的全长代表序列均已从冈比亚按蚊这一单一物种中分离出来,并对其核苷酸序列进行了分析。除了插入特异性外,RT1和RT2还具有一些结构和序列特征,表明它们属于类LINE(长散在核元件)或非长末端重复逆转座子,即编码逆转录酶的可移动元件类别。这些特征包括两个长的重叠开放阅读框(ORF)、poly(A)尾、不存在长末端重复序列以及大多数拷贝的5'端截短不均一。这两个元件的第一个ORF,尤其是RT1的ORF1,富含谷氨酰胺,并且包含长段的多聚谷氨酰胺,让人联想到opa重复序列。在羧基末端附近,ORF1中出现三个半胱氨酸 - 组氨酸基序,ORF2中出现一个。此外,每个ORF2都包含一个与逆转录酶和整合酶具有序列相似性的区域。RT1和RT2的蛋白质序列比对显示,在ORF1全长上有36%的同一性,在ORF2全长上有60%的同一性,但在5'和3'非编码区无法进行比对。与RT2不同,RT1的5'非编码区包含3.5个500个碱基对的亚重复序列拷贝,后面跟着一个poly(T)序列和两个不完美的55个碱基对的亚重复序列,第二个亚重复序列跨越ORF1的起始部分。这些元件在冈比亚按蚊复合体的五个亲缘物种中的分布模式并不均匀。RT1存在于实验室饲养和野生的冈比亚按蚊、阿拉伯按蚊和梅拉斯按蚊中,但在四带按蚊或梅鲁斯按蚊中未检测到。RT2在除梅鲁斯按蚊外的冈比亚按蚊复合体的所有可用成员中均已被检测到。拷贝数会波动,即使在单个野生雌性冈比亚按蚊的后代中也是如此。这些发现反映了一个复杂的进化历史,即在数百万年的时间里,在同一物种中,拷贝数的增减与两个竞争保守靶位点的元件的共存之间保持平衡。