Danilevskaya O N, Traverse K L, Hogan N C, DeBaryshe P G, Pardue M L
Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
Mol Cell Biol. 1999 Jan;19(1):873-81. doi: 10.1128/MCB.19.1.873.
The transposable elements HeT-A and TART constitute the telomeres of Drosophila chromosomes. Both are non-long terminal repeat (LTR) retrotransposons, sharing the remarkable property of transposing only to chromosome ends. In addition, strong sequence similarity of their gag proteins indicates that these coding regions share a common ancestor. These findings led to the assumption that HeT-A and TART are closely related. However, we now find that these elements produce quite different sets of transcripts. HeT-A produces only sense-strand transcripts of the full-length element, whereas TART produces both sense and antisense full-length RNAs, with antisense transcripts in more than 10-fold excess over sense RNA. In addition, features of TART sequence organization resemble those of a subclass of non-LTR elements characterized by unequal terminal repeats. Thus, the ancestral gag sequence appears to have become incorporated in two different types of elements, possibly with different functions in the telomere. HeT-A transcripts are found in both nuclear and cytoplasmic cell fractions, consistent with roles as both mRNA and transposition template. In contrast, both sense and antisense TART transcripts are almost entirely concentrated in nuclear fractions. Also, TART open reading frame 2 probes detect a cytoplasmic mRNA for reverse transcriptase (RT), with no similarity to TART sequence 5' or 3' of the RT coding region. This RNA could be a processed TART transcript or the product of a "free-standing" RT gene. Either origin would be novel. The distinctive transcription patterns of both HeT-A and TART are conserved in Drosophila yakuba, despite significant sequence divergence. The conservation argues that these sets of transcripts are important to the function(s) of HeT-A and TART.
转座元件HeT-A和TART构成了果蝇染色体的端粒。二者均为非长末端重复(LTR)逆转录转座子,具有仅转座至染色体末端的显著特性。此外,它们的gag蛋白具有高度的序列相似性,表明这些编码区域拥有共同的祖先。这些发现促使人们假定HeT-A和TART密切相关。然而,我们现在发现这些元件产生的转录本截然不同。HeT-A仅产生全长元件的正义链转录本,而TART则产生正义和反义全长RNA,其中反义转录本的数量超过正义RNA十倍以上。此外,TART序列组织的特征类似于一类以不等末端重复为特征的非LTR元件。因此,祖先的gag序列似乎已整合到两种不同类型的元件中,可能在端粒中具有不同的功能。HeT-A转录本在细胞核和细胞质细胞组分中均有发现,这与它们作为mRNA和转座模板的作用相一致。相比之下,TART的正义和反义转录本几乎完全集中在细胞核组分中。此外,TART开放阅读框2探针检测到一种细胞质中的逆转录酶(RT)mRNA,其与RT编码区域5'或3'端的TART序列没有相似性。这种RNA可能是加工后的TART转录本,也可能是一个“独立”RT基因的产物。无论哪种来源都是新颖的。尽管存在显著的序列差异,但HeT-A和TART独特的转录模式在雅库布果蝇中得以保留。这种保留表明这些转录本对HeT-A和TART的功能很重要。