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P细胞型和合子编码的阻遏蛋白对P-M杂种不育中转座抑制的模型。

Models of repression of transposition in P-M hybrid dysgenesis by P cytotype and by zygotically encoded repressor proteins.

作者信息

Brookfield J F

机构信息

Department of Genetics, University of Nottingham, Queens Medical Centre, England.

出版信息

Genetics. 1991 Jun;128(2):471-86. doi: 10.1093/genetics/128.2.471.

Abstract

By analytical theory and computer simulation the expected evolutionary dynamics of P transposable element spread in an infinite population are investigated. The analysis is based on the assumption that, unlike transposable elements which move via RNA intermediates, the harmful effects of P elements arise primarily in the act of transposition, and that this causes their evolutionary dynamics to be unusual. It is suggested that a situation of transposition-selection balance will be superceded by the buildup of a cytoplasmically inherited repression or by the elimination of active transposase-encoding elements from the chromosomes, a process which may be accompanied by the evolution of elements which encode proteins which repress transposition.

摘要

通过分析理论和计算机模拟,研究了P转座元件在无限种群中传播的预期进化动力学。该分析基于以下假设:与通过RNA中间体移动的转座元件不同,P元件的有害影响主要出现在转座过程中,这导致它们的进化动力学不同寻常。研究表明,转座-选择平衡的情况将被细胞质遗传抑制的积累或染色体上活性转座酶编码元件的消除所取代,这一过程可能伴随着编码抑制转座蛋白的元件的进化。

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