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HCN4离子通道功能对于以与节点和Lefty不对称基因表达无关的方式调节解剖学左右模式的早期事件是必需的。

HCN4 ion channel function is required for early events that regulate anatomical left-right patterning in a nodal and lefty asymmetric gene expression-independent manner.

作者信息

Pai Vaibhav P, Willocq Valerie, Pitcairn Emily J, Lemire Joan M, Paré Jean-François, Shi Nian-Qing, McLaughlin Kelly A, Levin Michael

机构信息

Allen Discovery Center at Tufts University, 200 Boston Ave, Suite 4600, Medford, MA 02155, USA.

Department of Medicine at University of Wisconsin-Madison, Madison, WI 53792, USA.

出版信息

Biol Open. 2017 Oct 15;6(10):1445-1457. doi: 10.1242/bio.025957.

Abstract

Laterality is a basic characteristic of all life forms, from single cell organisms to complex plants and animals. For many metazoans, consistent left-right asymmetric patterning is essential for the correct anatomy of internal organs, such as the heart, gut, and brain; disruption of left-right asymmetry patterning leads to an important class of birth defects in human patients. Laterality functions across multiple scales, where early embryonic, subcellular and chiral cytoskeletal events are coupled with asymmetric amplification mechanisms and gene regulatory networks leading to asymmetric physical forces that ultimately result in distinct left and right anatomical organ patterning. Recent studies have suggested the existence of multiple parallel pathways regulating organ asymmetry. Here, we show that an isoform of the hyperpolarization-activated cyclic nucleotide-gated (HCN) family of ion channels (hyperpolarization-activated cyclic nucleotide-gated channel 4, HCN4) is important for correct left-right patterning. HCN4 channels are present very early in embryos. Blocking HCN channels ( currents) with pharmacological inhibitors leads to errors in organ situs. This effect is only seen when HCN4 channels are blocked early (pre-stage 10) and not by a later block (post-stage 10). Injections of (dominant-negative) mRNA induce left-right defects only when injected in both blastomeres no later than the 2-cell stage. Analysis of key asymmetric genes' expression showed that the sidedness of , , and expression is largely unchanged by HCN4 blockade, despite the randomization of subsequent organ situs, although the area of expression was significantly reduced. Together these data identify a novel, developmental role for HCN4 channels and reveal a new asymmetric gene expression-independent mechanism upstream of organ positioning during embryonic left-right patterning.

摘要

从单细胞生物到复杂的植物和动物,左右不对称性是所有生命形式的一个基本特征。对于许多后生动物来说,一致的左右不对称模式对于心脏、肠道和大脑等内部器官的正确解剖结构至关重要;左右不对称模式的破坏会导致人类患者出现一类重要的出生缺陷。左右不对称性在多个尺度上发挥作用,早期胚胎、亚细胞和手性细胞骨架事件与不对称放大机制和基因调控网络相互耦合,导致不对称的物理力,最终产生明显的左右解剖器官模式。最近的研究表明存在多种平行途径调节器官不对称性。在这里,我们表明离子通道超极化激活环核苷酸门控(HCN)家族的一种亚型(超极化激活环核苷酸门控通道4,HCN4)对于正确的左右模式形成很重要。HCN4通道在胚胎早期就存在。用药物抑制剂阻断HCN通道(电流)会导致器官位置错误。这种效应只有在早期(10期之前)阻断HCN4通道时才会出现,而后期阻断(10期之后)则不会出现。仅在不晚于2细胞期将(显性负性)mRNA注射到两个卵裂球中时,才会诱导左右缺陷。对关键不对称基因表达的分析表明,尽管随后器官位置随机化,但HCN4阻断对Nodal、Lefty和Shh表达的偏向性影响不大,尽管Shh表达区域显著减少。这些数据共同确定了HCN4通道在发育中的新作用,并揭示了胚胎左右模式形成过程中器官定位上游一种新的与不对称基因表达无关的机制。

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