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

被引:32
作者
Hoshijima, K [1 ]
Metherall, JE [1 ]
Grunwald, DJ [1 ]
机构
[1] Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA
关键词
PDI; laterality patterning; midline; heart morphogenesis;
D O I
10.1101/gad.1001302
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:2518 / 2529
页数:12
相关论文
共 62 条
[1]  
Bisgrove BW, 2000, DEVELOPMENT, V127, P3567
[2]  
Bisgrove BW, 1999, DEVELOPMENT, V126, P3253
[3]   Classification of left-right patterning defects in zebrafish, mice, and humans [J].
Bisgrove, BW ;
Yost, HJ .
AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 101 (04) :315-323
[4]   The thyroid hormone-induced tail resorption program during Xenopus laevis metamorphosis [J].
Brown, DD ;
Wang, Z ;
Furlow, JD ;
Kanamori, A ;
Schwartzman, RA ;
Remo, BF ;
Pinder, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (05) :1924-1929
[5]  
Burdine RD, 2000, GENE DEV, V14, P763
[6]   Mechanisms of left-right determination in vertebrates [J].
Capdevila, J ;
Vogan, KJ ;
Tabin, CJ ;
Belmonte, JCI .
CELL, 2000, 101 (01) :9-21
[7]  
Chen JN, 1997, DEVELOPMENT, V124, P4373
[8]  
Chen JN, 1996, DEVELOPMENT, V122, P3809
[9]   Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function [J].
Chiang, C ;
Ying, LTT ;
Lee, E ;
Young, KE ;
Corden, JL ;
Westphal, H ;
Beachy, PA .
NATURE, 1996, 383 (6599) :407-413
[10]   Heart and gut chiralities are controlled independently from initial heart position in the developing zebrafish [J].
Chin, AJ ;
Tsang, M ;
Weinberg, ES .
DEVELOPMENTAL BIOLOGY, 2000, 227 (02) :403-421