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Analysis of the DNA and RNA changes associated with the expression of isotypic variant-specific antigens of trypanosomesd

机译:分析与锥虫体同型变异特异性抗原表达相关的DNA和RNA变化

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Using specific (32P) labelled cDNA probes, we compared the mRNAs and the genomic DNA sequences coding for the synthesis of two pairs of serologically related variant-specific antigens (VSAs) of trypanosomes : AnTat 1.1 and AnTat 1.1b, both from the strain 1125 of T.b.brucei and AnTat 1.8 and LiTat 1.6 from T.b.brucei and T.b. gambiense, respectively. Within each pair, large similarities were observed in the coding sequence, except in the 3′ region which appears to be highly variable. However, a low level of cross-hybridization can be detected between all sequences, in the 3′ region only. The expression of these VSAs is linked to a similar duplication-transposition mechanism. The insertion locus of the transposition unit is the same both in AnTat 1.1 and AnTat 1.1b DNAs. In both pairs, the transposition unit seems to comprise at least about 200 bp upstream of the 5′ extremity of the coding sequence. The significance of these results, regarding the structure and synthesis of the VSAs, is discussed.
机译:使用特异性( 32 P)标记的cDNA探针,我们比较了编码两对锥虫的血清学相关变体特异性抗原(VSA)的合成的mRNA和基因组DNA序列:AnTat 1.1和AnTat 1.1b,均来自Tbbrucei和AnTat 1.8的菌株1125和来自Tbbrucei和Tb的LiTat 1.6 gambiense,分别。在每一对中,在编码序列中观察到了很大的相似性,除了在3'区域中似乎高度可变之外。然而,仅在3'区域中可以在所有序列之间检测到低水平的交叉杂交。这些VSA的表达与相似的复制转座机制相关。在AnTat 1.1和AnTat 1.1b DNA中,转座单位的插入位点相同。在两对中,转座单元似乎在编码序列的5'末端上游至少包含约200 bp。讨论了这些结果对于VSA的结构和合成的意义。

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