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端粒重复序列内的同源重组在恶性疟原虫中产生染色体大小多态性。

Homologous recombination within subtelomeric repeat sequences generates chromosome size polymorphisms in P. falciparum.

作者信息

Corcoran L M, Thompson J K, Walliker D, Kemp D J

机构信息

Walter and Eliza Hall Institute of Medical Research, Victoria, Australia.

出版信息

Cell. 1988 Jun 3;53(5):807-13. doi: 10.1016/0092-8674(88)90097-9.

Abstract

We present restriction maps for chromosomes 1 and 2 of six cloned lines of P. falciparum. These delineate the locations of eight genetic markers, including genes for five antigens. In parasites from diverse areas, chromosome structure is conserved in central regions but is polymorphic both in length and sequence near the telomeres. The telomeres and adjacent sequences comprise a conserved structure at the ends of most P. falciparum chromosomes. However, the subtelomeric zones are polymorphic and coincide with the locations of a repetitive element (rep20). Deletions of rep20 generate clones of P. falciparum that lack rep20 on one or both ends of chromosomes 1 or 2, and larger deletions remove telomere-proximal genes as well. The chromosome length polymorphisms can therefore be largely explained by recombination within these blocks of repeats, a mechanism that is also important in the generation of diversity in genes for repetitive antigens of P. falciparum.

摘要

我们展示了恶性疟原虫六个克隆系1号和2号染色体的限制性图谱。这些图谱描绘了八个遗传标记的位置,包括五个抗原的基因。在来自不同地区的疟原虫中,染色体结构在中心区域是保守的,但在端粒附近的长度和序列上是多态的。端粒和相邻序列在大多数恶性疟原虫染色体末端构成一个保守结构。然而,亚端粒区域是多态的,并且与一个重复元件(rep20)的位置重合。rep20的缺失产生了在1号或2号染色体一端或两端缺少rep20的恶性疟原虫克隆,更大的缺失也会去除端粒近端基因。因此,染色体长度多态性在很大程度上可以由这些重复序列块内的重组来解释,这一机制在恶性疟原虫重复抗原基因多样性的产生中也很重要。

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