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在发育中的斑马鱼中,心脏和肠道的手性是独立于初始心脏位置进行控制的。

Heart and gut chiralities are controlled independently from initial heart position in the developing zebrafish.

作者信息

Chin A J, Tsang M, Weinberg E S

机构信息

Department of Biology, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.

出版信息

Dev Biol. 2000 Nov 15;227(2):403-21. doi: 10.1006/dbio.2000.9924.

Abstract

A fundamental problem in developmental biology is how left-right (LR) asymmetry is generated, both on the whole organism level and at the level of an individual organ or structure. To investigate the relationship of organ sidedness to organ chirality, we examined 12 zebrafish mutants for initial heart tube position and later heart looping direction (chirality). Anomalous initial heart position was found in seven mutants, which also demonstrated loss of normal LR asymmetry in lateral plate mesoderm (LPM) antivin/lefty-1 and Pitx2 expression. Those with a relatively normal notochord (cyc(b16), din, and spt) displayed a predictive correlation between initial heart position and heart chirality, whereas initial heart position and heart chirality were independently randomized in those with a defective notochord (flh, boz, ntl, and mom). The predictability of heart chirality in spt, din, and b16 embryos, even in the absence of normal antivin/lefty-1 and Pitx2 expression, strongly suggests that heart chirality is controlled by a process distinct from that which controls appropriate left-sided LPM expression of antivin-Pitx2 signaling pathway molecules. In addition, there was correlation of initial heart position with gut chirality (and also between heart chirality and gut chirality) in the first class of mutants with normal notochord, but not in the second class, which appears to model human heterotaxy syndrome.

摘要

发育生物学中的一个基本问题是,左右(LR)不对称是如何在整个生物体水平以及单个器官或结构水平上产生的。为了研究器官的左右定位与器官手性之间的关系,我们检测了12个斑马鱼突变体的初始心脏管位置和后来的心脏环化方向(手性)。在7个突变体中发现了异常的初始心脏位置,这些突变体在侧板中胚层(LPM)抗维甲酸/左y-1和Pitx2表达中也表现出正常LR不对称性的丧失。那些脊索相对正常的突变体(cyc(b16)、din和spt)在初始心脏位置和心脏手性之间显示出预测性的相关性,而在那些脊索有缺陷的突变体(flh、boz、ntl和mom)中,初始心脏位置和心脏手性是独立随机的。即使在没有正常的抗维甲酸/左y-1和Pitx2表达的情况下,spt、din和b16胚胎中心脏手性的可预测性强烈表明,心脏手性是由一个与控制抗维甲酸-Pitx2信号通路分子在左侧LPM中正常表达的过程不同的过程所控制的。此外,在第一类脊索正常的突变体中,初始心脏位置与肠道手性相关(心脏手性与肠道手性之间也相关),但在第二类突变体中不相关,第二类突变体似乎模拟了人类内脏异位综合征。

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