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海胆胚胎发育过程中,tektin A mRNA的转录调控与纤毛发育及长度决定相关。

Transcriptional control of tektin A mRNA correlates with cilia development and length determination during sea urchin embryogenesis.

作者信息

Norrander J M, Linck R W, Stephens R E

机构信息

Department of Cell Biology and Neuroanatomy, University of Minnesota, Minneapolis 55455, USA.

出版信息

Development. 1995 Jun;121(6):1615-23. doi: 10.1242/dev.121.6.1615.

DOI:10.1242/dev.121.6.1615
PMID:7600979
Abstract

Previous studies have shown that tektin A, one of three integral filamentous protein components of outer doublet microtubules, is synthesized in sea urchins in an amount correlating to the length of embryonic cilia initially assembled or experimentally regenerated. To investigate further the molecular mechanism for the regulation of tektin synthesis, tektin cDNA clones were used to assess mRNA levels during ciliogenesis, zinc-induced animalization, deciliation-induced regeneration and theophylline-induced elongation. Possibly involved in centriole replication, low, near-constant levels of mRNA for all three tektins are present in the unfertilized egg and during cleavage stages. Preceded by new synthesis of tektin B and C mRNAs, tektin A mRNA is up-regulated during ciliogenesis, but only tektin A mRNA levels correlate directly with ciliary length in animalized embryos; the others augment larger, non-limiting pools of tektins B and C. Tektin mRNAs decrease to steady-state levels after ciliogenesis, but are up-regulated again when the embryos are deciliated, correlating with the length of cilia to be deployed. In a species where a 3-fold ciliary length increase can be induced by theophylline treatment of zinc-arrested embryos, the mRNAs accumulate to proportionately higher levels during arrest but are not translated until induction, whereupon they decrease inversely with ciliary elongation. This suggests transcriptional control with respect to mRNA amounts but post-transcriptional control with respect to the expression of this phenotype.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

先前的研究表明,纤毛蛋白A是外双联微管三种完整丝状蛋白成分之一,在海胆中的合成量与最初组装或实验再生的胚胎纤毛长度相关。为了进一步研究纤毛蛋白合成调控的分子机制,利用纤毛蛋白cDNA克隆来评估纤毛发生、锌诱导的动物化、去纤毛诱导的再生以及茶碱诱导的伸长过程中的mRNA水平。所有三种纤毛蛋白的mRNA在未受精卵和卵裂阶段含量较低且近乎恒定,可能参与中心粒复制。在纤毛蛋白B和C的mRNA重新合成之后,纤毛蛋白A的mRNA在纤毛发生过程中上调,但在动物化胚胎中只有纤毛蛋白A的mRNA水平与纤毛长度直接相关;其他的则增加了更大的、非限制性的纤毛蛋白B和C库。纤毛蛋白mRNA在纤毛发生后降至稳态水平,但当胚胎去纤毛时又上调,这与即将形成的纤毛长度相关。在一个物种中,用茶碱处理锌阻滞的胚胎可使纤毛长度增加3倍,mRNA在阻滞期间积累到相应更高的水平,但直到诱导时才翻译,随后随着纤毛伸长而反向减少。这表明在mRNA量方面存在转录控制,但在该表型的表达方面存在转录后控制。(摘要截选至250字)

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Transcriptional control of tektin A mRNA correlates with cilia development and length determination during sea urchin embryogenesis.海胆胚胎发育过程中,tektin A mRNA的转录调控与纤毛发育及长度决定相关。
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