Bringaud Frederic, Biteau Nicolas, Melville Sara E, Hez Stéphanie, El-Sayed Najib M, Leech Vanessa, Berriman Matthew, Hall Neil, Donelson John E, Baltz Théo
Laboratoire de Parasitologie Moléculaire, Université Victor Segalen Bordeaux II, UMR-5016 CNRS, 33076 Bordeaux, France.
Eukaryot Cell. 2002 Feb;1(1):137-51. doi: 10.1128/EC.1.1.137-151.2002.
We describe a novel gene family that forms clusters in subtelomeric regions of Trypanosoma brucei chromosomes and partially accounts for the observed clustering of retrotransposons. The ingi and ribosomal inserted mobile element (RIME) non-LTR retrotransposons share 250 bp at both extremities and are the most abundant putatively mobile elements, with about 500 copies per haploid genome. From cDNA clones and subsequently in the T. brucei genomic DNA databases, we identified 52 homologous gene and pseudogene sequences, 16 of which contain a RIME and/or ingi retrotransposon inserted at exactly the same relative position. Here these genes are called the RHS family, for retrotransposon hot spot. Comparison of the protein sequences encoded by RHS genes (21 copies) and pseudogenes (24 copies) revealed a conserved central region containing an ATP/GTP-binding motif and the RIME/ingi insertion site. The RHS proteins share between 13 and 96% identity, and six subfamilies, RHS1 to RHS6, can be defined on the basis of their divergent C-terminal domains. Immunofluorescence and Western blot analyses using RHS subfamily-specific immune sera show that RHS proteins are constitutively expressed and occur mainly in the nucleus. Analysis of Genome Survey Sequence databases indicated that the Trypanosoma brucei diploid genome contains about 280 RHS (pseudo)genes. Among the 52 identified RHS (pseudo)genes, 48 copies are in three RHS clusters located in subtelomeric regions of chromosomes Ia and II and adjacent to the active bloodstream form expression site in T. brucei strain TREU927/4 GUTat10.1. RHS genes comprise the remaining sequence of the size-polymorphic "repetitive region" described for T. brucei chromosome I, and a homologous gene family is present in the Trypanosoma cruzi genome.
我们描述了一个新的基因家族,该家族在布氏锥虫染色体的亚端粒区域形成簇,部分解释了观察到的逆转录转座子的聚集现象。ingi和核糖体插入移动元件(RIME)非LTR逆转录转座子在两端共享250 bp,是最丰富的假定可移动元件,每个单倍体基因组约有500个拷贝。从cDNA克隆以及随后在布氏锥虫基因组DNA数据库中,我们鉴定出52个同源基因和假基因序列,其中16个在完全相同的相对位置插入了RIME和/或ingi逆转录转座子。在这里,这些基因被称为RHS家族,即逆转录转座子热点。对RHS基因(21个拷贝)和假基因(24个拷贝)编码的蛋白质序列进行比较,发现一个保守的中央区域,其中包含一个ATP/GTP结合基序和RIME/ingi插入位点。RHS蛋白的同一性在13%至96%之间,根据其不同的C末端结构域可定义六个亚家族,即RHS1至RHS6。使用RHS亚家族特异性免疫血清进行的免疫荧光和蛋白质印迹分析表明,RHS蛋白组成性表达,主要存在于细胞核中。对基因组调查序列数据库的分析表明,布氏锥虫二倍体基因组包含约280个RHS(假)基因。在鉴定出的52个RHS(假)基因中,48个拷贝位于染色体Ia和II亚端粒区域的三个RHS簇中,并且与布氏锥虫菌株TREU927/4 GUTat10.1中活跃的血流形式表达位点相邻。RHS基因构成了布氏锥虫染色体I所描述的大小多态性“重复区域”的其余序列,并且在克氏锥虫基因组中存在一个同源基因家族。