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恶性疟原虫的11-1基因编码不同的快速进化重复序列。

The 11-1 gene of Plasmodium falciparum codes for distinct fast evolving repeats.

作者信息

Scherf A, Hilbich C, Sieg K, Mattei D, Mercereau-Puijalon O, Müller-Hill B

机构信息

Institut für Genetik der Universität zu Köln, FRG.

出版信息

EMBO J. 1988 Apr;7(4):1129-37. doi: 10.1002/j.1460-2075.1988.tb02922.x.

Abstract

The 11-1 gene of Plasmodium falciparum has been investigated by DNA sequence analysis. It begins at the 5' end with a putative miniexon coding for a polypeptide which has the characteristics of a signal sequence. The miniexon is followed by a small intron. This again is followed by a large exon consisting of 9-, 18- and 27-bp repeats embedded in unique DNA. Specific antibodies isolated by affinity chromatography on a purified recombinant fusion protein expressing the three- and six-amino acid repeats were used to identify the product of the 11-1 gene. In exhibits size variations from 260 to 350 kd in different strains. Southern blot analysis with synthetic DNA as probe demonstrates that the 18-bp repeat is absent or drastically altered in two strains whereas the other repeats are present in all seven strains investigated. The unusual preference for G in the third position of some codons of the repeats but not in the unique sequences indicates rapid evolution of the repeats. Slippage during replication, unequal crossing over and selection are discussed as possible mechanisms leading rapidly to extreme diversity.

摘要

通过DNA序列分析对恶性疟原虫的11 - 1基因进行了研究。它从5'端开始,有一个假定的小外显子,编码一种具有信号序列特征的多肽。小外显子后接一个小内含子。接着是一个大外显子,由嵌入独特DNA中的9个、18个和27个碱基对的重复序列组成。通过在表达三氨基酸和六氨基酸重复序列的纯化重组融合蛋白上进行亲和层析分离得到的特异性抗体,用于鉴定11 - 1基因的产物。在不同菌株中,其大小在260至350kd之间变化。以合成DNA为探针的Southern印迹分析表明,在两个菌株中18个碱基对的重复序列缺失或发生了显著改变,而在所有研究的七个菌株中其他重复序列均存在。重复序列某些密码子第三位对G的异常偏好,而独特序列中则没有这种偏好,这表明重复序列的快速进化。复制过程中的滑动、不等交换和选择被讨论为可能导致快速极端多样性的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a42e/454447/a7f72ec93d4e/emboj00141-0244-a.jpg

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