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本文引用的文献

1
Establishment of vertebrate left-right asymmetry.脊椎动物左右不对称性的建立。
Nat Rev Genet. 2002 Feb;3(2):103-13. doi: 10.1038/nrg732.
2
Midline and laterality defects: left and right meet in the middle.中线和侧方缺损:左右在中间会合。
Bioessays. 2001 Oct;23(10):888-900. doi: 10.1002/bies.1130.
3
Classification of left-right patterning defects in zebrafish, mice, and humans.斑马鱼、小鼠和人类左右模式缺陷的分类。
Am J Med Genet. 2001 Jul 15;101(4):315-23. doi: 10.1002/ajmg.1180.
4
The gene encoding a newly discovered protein, chorein, is mutated in chorea-acanthocytosis.编码新发现的蛋白质—— chorein 的基因在舞蹈病 - 棘红细胞增多症中发生突变。
Nat Genet. 2001 Jun;28(2):121-2. doi: 10.1038/88825.
5
A conserved sorting-associated protein is mutant in chorea-acanthocytosis.一种保守的分选相关蛋白在舞蹈病-棘红细胞增多症中发生突变。
Nat Genet. 2001 Jun;28(2):119-20. doi: 10.1038/88821.
6
Zebrafish genetics and vertebrate heart formation.斑马鱼遗传学与脊椎动物心脏形成
Nat Rev Genet. 2001 Jan;2(1):39-48. doi: 10.1038/35047564.
7
A nodal signaling pathway regulates the laterality of neuroanatomical asymmetries in the zebrafish forebrain.一条节点信号通路调节斑马鱼前脑神经解剖不对称性的左右侧性。
Neuron. 2000 Nov;28(2):399-409. doi: 10.1016/s0896-6273(00)00120-3.
8
Windbeutel is required for function and correct subcellular localization of the Drosophila patterning protein Pipe.风袋蛋白对于果蝇模式形成蛋白管道的功能和正确的亚细胞定位是必需的。
Development. 2000 Dec;127(24):5541-50. doi: 10.1242/dev.127.24.5541.
9
Heart and gut chiralities are controlled independently from initial heart position in the developing zebrafish.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。
Dev Biol. 2000 Nov 15;227(2):403-21. doi: 10.1006/dbio.2000.9924.
10
Asymmetric nodal signaling in the zebrafish diencephalon positions the pineal organ.斑马鱼间脑中的不对称节点信号定位松果体器官。
Development. 2000 Dec;127(23):5101-12. doi: 10.1242/dev.127.23.5101.

胚胎中线表达的一种蛋白质二硫键异构酶是左右不对称所必需的。

A protein disulfide isomerase expressed in the embryonic midline is required for left/right asymmetries.

作者信息

Hoshijima Kazuyuki, Metherall James E, Grunwald David Jonah

机构信息

Department of Human Genetics, University of Utah, Salt Lake City, Utah 84112, USA.

出版信息

Genes Dev. 2002 Oct 1;16(19):2518-29. doi: 10.1101/gad.1001302.

DOI:10.1101/gad.1001302
PMID:12368263
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC187449/
Abstract

Although the vertebrate embryonic midline plays a critical role in determining the left/right asymmetric development of multiple organs, few genes expressed in the midline are known to function specifically in establishing laterality patterning. Here we show that a gene encoding protein disulfide isomerase P5 (PDI-P5) is expressed at high levels in the organizer and axial mesoderm and is required for establishing left/right asymmetries in the zebrafish embryo. pdi-p5 was discovered in a screen to detect genes down-regulated in the zebrafish midline mutant one-eyed pinhead and expressed predominantly in midline tissues of wild-type embryos. Depletion of the pdi-p5 product with morpholino antisense oligonucleotides results in loss of the asymmetric development of the heart, liver, pancreas, and gut. In addition, PDI-P5 depletion results in bilateral expression of all genes known to be expressed asymmetrically in the lateral plate mesoderm and the brain during embryogenesis. The laterality defects caused by pdi-p5 antisense treatment arise solely due to loss of the PDI-P5 protein, as they are reversed when treated embryos are supplied with an exogenous source of the PDI-P5 protein. Thus the spectrum of laterality defects resulting from depletion of the PDI-P5 protein fully recapitulates that resulting from loss of the midline. As loss of PDI-P5 does not appear to interfere with other aspects of midline development or function, we propose that PDI-P5 is specifically involved in the production of midline-derived signals required to establish left/right asymmetry.

摘要

尽管脊椎动物胚胎中线在决定多个器官的左右不对称发育中起着关键作用,但已知在中线表达的基因中,很少有基因在建立左右模式中具有特定功能。在这里,我们表明,一个编码蛋白质二硫键异构酶P5(PDI-P5)的基因在组织者和轴中胚层中高水平表达,并且是斑马鱼胚胎建立左右不对称所必需的。pdi-p5是在一个筛选中发现的,该筛选用于检测斑马鱼中线突变体“独眼针头”中下调的基因,并且主要在野生型胚胎的中线组织中表达。用吗啉代反义寡核苷酸耗尽pdi-p5产物会导致心脏、肝脏、胰腺和肠道的不对称发育丧失。此外,PDI-P5的耗尽导致所有已知在胚胎发育过程中在侧板中胚层和大脑中不对称表达的基因的双侧表达。pdi-p5反义处理引起的左右缺陷完全是由于PDI-P5蛋白的丧失所致,因为当给处理过的胚胎提供外源性PDI-P5蛋白时,这些缺陷会被逆转。因此,PDI-P5蛋白耗尽导致的左右缺陷谱完全概括了中线丧失导致的缺陷谱。由于PDI-P5的丧失似乎不会干扰中线发育或功能的其他方面,我们提出PDI-P5特别参与建立左右不对称所需的中线衍生信号的产生。