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嗜热四膜虫的双向突变所指定的镜像模式是如何表达的。

How the mirror-image pattern specified by a janus mutation of Tetrahymena thermophila comes to expression.

作者信息

Frankel J, Nelsen E M

机构信息

Department of Biology, University of Iowa, Iowa City 52242.

出版信息

Dev Genet. 1986;6(3):213-38. doi: 10.1002/dvg.1020060306.

Abstract

The initial changes of cell-surface organization that occurred as the recessive janA1 (janus) mutation of Tetrahymena thermophila first became expressed were elucidated in a special mating scheme in which old macronuclei homozygous for janA+ were synchronously replaced by new macronuclei homozygous for janA1. During this period of onset of expression, the number, regularity, and asymmetry of the ciliary rows remained unchanged. New normal (primary) oral apparatuses (OAs) continued to be formed posterior to old OAs, as in normal cells. At about four fissions after conjugation, abnormal (secondary) OAs with a partial reversal of asymmetry began to appear nearly opposite to the primary OAs, close to but not at the eventual circumferential position of janA1 secondary OAs. The array of contractile vacuole pores (CVPs), normally located adjacent to two ciliary rows centered near 22% of the cell circumference to the right of the primary oral meridian, underwent a two-step transformation: first, the number of adjacent ciliary rows bearing CVPs increased to 3, 4, and sometimes 5, then "skipped" rows appeared within this broadened CVP-arc to split the single set of CVPs into two separated subsets. The CVP transformations occurred gradually and progressively. They began prior to the expression of secondary OAs but accelerated as secondary OAs appeared. As the CVP arc became broader, its midpoint shifted somewhat to the right, away from the primary oral meridian, but ended up close to halfway between the primary and secondary oral meridians. The data provide a better fit to an intercalation model than to an alternative double-gradient model, suggesting that the janA1 mutation alters the large-scale organization of positional values by preventing the expression of a subset of these values and thus provoking reverse-intercalation of the remainder.

摘要

嗜热四膜虫隐性janA1(雅努斯)突变首次表达时细胞表面组织的初始变化,是在一种特殊的交配方案中阐明的,在该方案中,janA +纯合的旧大核被janA1纯合的新大核同步取代。在表达开始的这段时间里,纤毛排的数量、规则性和不对称性保持不变。新的正常(初级)口器(OAs)继续在旧口器后方形成,就像在正常细胞中一样。在接合后大约四次分裂时,不对称性部分反转的异常(次级)口器开始出现在几乎与初级口器相对的位置,靠近但不在janA1次级口器最终的圆周位置。收缩泡孔(CVPs)阵列通常位于靠近细胞周长22%、初级口子午线右侧中心的两排纤毛附近,经历了两步转变:首先,带有CVPs的相邻纤毛排数量增加到3、4,有时为5排,然后在这个变宽的CVP弧内出现“跳跃”排,将单组CVPs分成两个分开的子集。CVP转变是逐渐发生且逐步进行的。它们在次级口器表达之前就开始了,但随着次级口器的出现而加速。随着CVP弧变宽,其中点稍微向右移动,远离初级口子午线,但最终接近初级和次级口子午线之间的中点。这些数据更符合插入模型,而不是替代的双梯度模型,这表明janA1突变通过阻止这些值的一个子集的表达,从而引发其余部分的反向插入,改变了位置值的大规模组织。

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