Aline R F, Scholler J K, Stuart K
Seattle Biomedical Research Institute, WA 98109.
Mol Biochem Parasitol. 1989 Jan 15;32(2-3):169-78. doi: 10.1016/0166-6851(89)90068-6.
In Trypanosoma brucei the 5' proximal flanking sequences of a variant surface glycoprotein (VSG) gene, the co-transposed segment, are transcribed in a variant antigenic type- and stage-specific fashion along with the VSG gene. The precursor transcripts are subsequently processed to yield smaller transcripts from the co-transposed segment as well as the VSG mRNA. These co-transposed segment transcripts are quite abundant, polyadenylated and contain the spliced leader sequence, all characteristics of trypanosome mRNAs. We have found that all of the co-transposed segment transcripts from two VSG genes are present in polyribosomes. The nucleotide sequence of much of the co-transposed segment of one of these VSG genes, however, has no open reading frames coding for proteins longer than 49 amino acids. These results suggest that co-transposed segment transcripts do not encode essential proteins even though they are present in polyribosomes and may be translated.
在布氏锥虫中,可变表面糖蛋白(VSG)基因5'近端侧翼序列,即共转座区段,与VSG基因一起以可变抗原类型和阶段特异性方式转录。前体转录本随后被加工,从共转座区段以及VSG mRNA产生较小的转录本。这些共转座区段转录本相当丰富,进行了多聚腺苷酸化并且含有剪接前导序列,这些都是锥虫mRNA的特征。我们发现来自两个VSG基因的所有共转座区段转录本都存在于多核糖体中。然而,其中一个VSG基因的大部分共转座区段的核苷酸序列没有编码长度超过49个氨基酸的蛋白质的开放阅读框。这些结果表明,共转座区段转录本即使存在于多核糖体中并且可能被翻译,也不编码必需蛋白质。