拟南芥中一个具有特殊结构特征的新品系(ATLN-L)。

K. Noma, H. Ohtsubo, E. Ohtsubo
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引用次数: 5

摘要

拟南芥基因组有大约250个LINEs拷贝(这里称为atln)。其中,一些被称为atln - l,在两个连续的开放阅读帧orf1和orf2的下游区域有一个大约2kb的额外序列。有趣的是,这些ATLN-L成员中的额外序列有另一个开放阅读框,命名为orf3。每个成员的两侧都有一个目标位点序列的直接重复,表明具有三个开放阅读框的ATLN-L成员作为一个单元进行了反转录。ATLN- l成员也与其他ATLN成员不同:orf1以TAA(或TAG)终止,与orf2位于同一帧中,orf2的ATG起始密码子不存在于近端区域。orf2的近端区存在一个可能在ATLN-L mRNA中形成伪结结构的序列,因此假设在翻译ATLN-L mRNA时,orf1的TAA(或TAG)终止密码子被抑制以产生orf1 - orf2转框蛋白。orf2和orf3之间的区域长达数百bp,表明orf3的表达与orfl-orf2无关。Orf1和Orf3蛋白的氨基酸序列在其具有逆转录病毒锌指基序的RNA结合的n端半区高度同源。然而,Orf3除了锌指图案外,还有亮氨酸拉链图案。Orf1和Orf3蛋白的c端同源性较差,但似乎具有核定位信号,提示这些蛋白参与了ATLN-L mRNA向细胞核的转移。系统发育树显示Orf3蛋白与ATLN-L成员编码的Orf1蛋白形成不同的分支。这表明,在进化过程中,ATLN- ls的一个祖先元件将另一个ATLN成员携带的orf1框架纳入了其远端orf1-orf2区域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A new class of LINEs (ATLN-L) from Arabidopsis thaliana with extraordinary structural features.
The Arabidopsis thaliana genome has about 250 copies of LINEs (here called ATLNs). Of these, some, called ATLN-Ls, have an extra sequence of about 2 kb in the region downstream of two consecutive open reading frames, orf1 and orf2. Interestingly, the extra sequences in these ATLN-L members have another open reading frame, designated as orf3. Each member is flanked by direct repeats of a target site sequence, showing that ATLN-L members with the three open reading frames have retrotransposed as a unit. The ATLN-L members are also distinct from other ATLN members: orf1 terminates with TAA (or TAG) and is located in the same frame as orf2, and the ATG initiation codon of orf2 is not present in the proximal region. A sequence that may form a pseudoknot structure in ATLN-L mRNA was present in the proximal region of orf2, therefore the TAA (or TAG) termination codon of orf1 is assumed to be suppressed to produce an Orf1-Orf2 transframe protein during the translation of the ATLN-L mRNA. The region between orf2 and orf3 is several hundred bp long, suggesting that orf3 expression is independent of orfl-orf2. The amino acid sequences of the proteins Orf1 and Orf3 are highly homologous in their N-terminal half regions that have a retroviral zinc-finger motif for RNA binding. Orf3, however, has a leucine-zipper motif in addition to the zinc-finger motif. The C-terminal regions of the Orf1 and Orf3 proteins have poor homology, but seem to have nuclear localization signals, suggesting that these proteins are involved in the transfer of ATLN-L mRNA to nuclei. A phylogenetic tree shows that Orf3 proteins form a branch distinct from the branches of the Orf1 proteins encoded by ATLN-L members. This indicates that an ancestor element of ATLN-Ls has incorporated the orf1 frame carried by another ATLN member into its distal region to orf1-orf2 during evolution.
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