Hoshijima Kazuyuki, Metherall James E, Grunwald David Jonah
Department of Human Genetics, University of Utah, Salt Lake City, Utah 84112, USA.
Genes Dev. 2002 Oct 1;16(19):2518-29. doi: 10.1101/gad.1001302.
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.
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。