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恶性疟原虫野外分离株的亚端粒染色体缺失及其与体外细胞黏附丧失的关系。

Subtelomeric chromosome deletions in field isolates of Plasmodium falciparum and their relationship to loss of cytoadherence in vitro.

作者信息

Biggs B A, Kemp D J, Brown G V

机构信息

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

出版信息

Proc Natl Acad Sci U S A. 1989 Apr;86(7):2428-32. doi: 10.1073/pnas.86.7.2428.

Abstract

Subtelomeric deletions are responsible for the loss of expression of several Plasmodium falciparum antigens, including the knob-associated histidine-rich protein (KAHRP). Such deletions are detectable by two-dimensional pulsed-field gradient electrophoresis (PFGE) in which the chromosomes separated in dimension 1 are cleaved with Apa I, and the sizes of telomeric fragments are determined in dimension 2. This sensitive technique has enabled us to examine the role of subtelomeric deletions in two aspects of the biology of Plasmodium falciparum. First, we show that similar subtelomeric deletions to those that occur in vitro also occur in field isolates. Second, we demonstrate a correlation between subtelomeric deletions and loss of the phenotype of "cytoadherence" in cultured isolates. Subclones were generated from the cytoadherent cloned isolate ItG2F6, and their phenotypes were examined with respect to cytoadherence, the expression of "knobs," and agglutination of infected erythrocytes with rabbit antiserum. The only chromosomal change detectable by two-dimensional PFGE among subclones that differ from wild type in each of these three characteristics is a deletion of approximately 100 kilobases at one end of chromosome 2. This deletion includes the gene coding for KAHRP and the subtelomeric repeat designated rep20.

摘要

亚端粒缺失导致了恶性疟原虫多种抗原表达的丧失,其中包括与结节相关的富含组氨酸蛋白(KAHRP)。这种缺失可通过二维脉冲场梯度电泳(PFGE)检测到,在该方法中,在第一维中分离的染色体用Apa I酶切,然后在第二维中确定端粒片段的大小。这种灵敏的技术使我们能够从两个方面研究亚端粒缺失在恶性疟原虫生物学中的作用。第一,我们发现体外出现的类似亚端粒缺失在野外分离株中也会发生。第二,我们证明了亚端粒缺失与培养分离株中“细胞黏附”表型丧失之间存在相关性。从具有细胞黏附性的克隆分离株ItG2F6中产生亚克隆,并针对细胞黏附、“结节”的表达以及感染红细胞与兔抗血清的凝集反应对其表型进行检测。在这三个特征中与野生型不同的亚克隆中,通过二维PFGE唯一可检测到的染色体变化是2号染色体一端大约100千碱基的缺失。该缺失包括编码KAHRP的基因和命名为rep20的亚端粒重复序列。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b43/286926/b7b9062fafd6/pnas00247-0315-a.jpg

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