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海胆SM50 C元件基因调控区域Onecut结合活性的实证模型。

An empirical model of Onecut binding activity at the sea urchin SM50 C-element gene regulatory region.

作者信息

Otim Ochan

机构信息

Division of Biology, California Institute of Technology, Pasadena, CA, USA.

出版信息

Int J Dev Biol. 2017;61(8-9):537-543. doi: 10.1387/ijdb.170194oo.

Abstract

Studying the formation of endoskeleton in many species is complex and difficult. The sea urchin embryo offers an unparalleled platform for understanding this process because of the ease with which its skeletogenic mesenchyme cells can be manipulated. In this study, preliminary evidence from biochemical studies towards understanding the role of the Onecut transcription factor during sea urchin skeletogenic mesenchyme cell specification is presented. Based on the evidence, an empirical model is proposed showing how Onecut, together with associated co-factors, may be using the C-element of the SM50 gene regulatory region in advance of the sea urchin Strongylocentrotus purpuratus spicule development. In the model, Onecut recognizes and binds the DNA sequence CATCGATCTC in the C-element without temporal restriction. Onecut then utilizes different sets of co-factors to switch from its unknown function early in development (four cell stage to the mesenchyme blastula stage), to its known role in the oral-aboral boundary thereafter. At the writing of this report, definitive evidence as to whether the "early" factors are expressed in all cells except the micromere lineages, or whether the "late" factors are expressed in micromere descendants or ectodermal precursors only are lacking. The former would suggest a possible Onecut repression function for the early co-factors outside the micromere lineages; the latter scenario would suggest a Onecut activation function for the late co-factors in the presumptive ciliary band.

摘要

研究许多物种中内骨骼的形成既复杂又困难。海胆胚胎为理解这一过程提供了一个无与伦比的平台,因为其造骨间充质细胞易于操控。在本研究中,展示了来自生化研究的初步证据,旨在了解Onecut转录因子在海胆造骨间充质细胞特化过程中的作用。基于这些证据,提出了一个经验模型,显示了Onecut如何与相关辅助因子一起,在紫球海胆针状体发育之前利用SM50基因调控区域的C元件。在该模型中,Onecut无时间限制地识别并结合C元件中的DNA序列CATCGATCTC。然后,Onecut利用不同的辅助因子组合,从发育早期(四细胞期到间充质囊胚期)的未知功能,转变为之后在口-反口边界的已知作用。在撰写本报告时,尚缺乏确凿证据来确定“早期”因子是否在除小分裂球谱系之外的所有细胞中表达,或者“晚期”因子是否仅在小分裂球后代或外胚层前体中表达。前一种情况可能表明早期辅助因子在小分裂球谱系之外具有Onecut抑制功能;后一种情况则可能表明晚期辅助因子在假定的纤毛带中具有Onecut激活功能。

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