Hao Limin, Mukherjee Krishanu, Liegeois Samuel, Baillie David, Labouesse Michel, Bürglin Thomas R
Department of Biosciences and Nutrition, and Center for Genomics and Bioinformatics, Karolinska Institutet, Huddinge, Sweden.
Dev Dyn. 2006 Jun;235(6):1469-81. doi: 10.1002/dvdy.20721.
The Caenorhabditis elegans genome encodes ten proteins that share similarity with Hedgehog through the C-terminal Hint/Hog domain. While most genes are members of larger gene families, qua-1 is a single copy gene. Here we show that orthologs of qua-1 exist in many nematodes, including Brugia malayi, which shared a common ancestor with C. elegans about 300 million years ago. The QUA-1 proteins contain an N-terminal domain, the Qua domain, that is highly conserved, but whose molecular function is not known. We have studied the expression pattern of qua-1 in C. elegans using a qua-1::GFP transcriptional fusion. qua-1 is mainly expressed in hyp1 to hyp11 hypodermal cells, but not in seam cells. It is also expressed in intestinal and rectal cells, sensilla support cells, and the P cell lineage in L1. The expression of qua-1::GFP undergoes cyclical changes during development in phase with the molting cycle. It accumulates prior to molting and disappears between molts. Disruption of the qua-1 gene function through an internal deletion that causes a frame shift with premature stop in the middle of the gene results in strong lethality. The animals arrest in the early larval stages due to defects in molting. Electron microscopy reveals double cuticles due to defective ecdysis, but no obvious defects are seen in the hypodermis. Qua domain-only::GFP and full-length QUA-1::GFP fusion constructs are secreted and associated with the overlying cuticle, but only QUA-1::GFP rescues the mutant phenotype. Our results suggest that both the Hint/Hog domain and Qua domain are critically required for the function of QUA-1.
秀丽隐杆线虫基因组编码十种通过C端Hint/Hog结构域与刺猬蛋白具有相似性的蛋白质。虽然大多数基因是较大基因家族的成员,但qua-1是一个单拷贝基因。我们在此表明,qua-1的直系同源基因存在于许多线虫中,包括马来布鲁线虫,它与秀丽隐杆线虫在约3亿年前拥有共同祖先。QUA-1蛋白包含一个N端结构域,即Qua结构域,该结构域高度保守,但其分子功能尚不清楚。我们使用qua-1::GFP转录融合研究了秀丽隐杆线虫中qua-1的表达模式。qua-1主要在hyp1至hyp11的皮下细胞中表达,但不在缝合细胞中表达。它也在肠和直肠细胞、感觉器支持细胞以及L1期的P细胞谱系中表达。qua-1::GFP的表达在发育过程中与蜕皮周期同步经历周期性变化。它在蜕皮前积累,并在蜕皮之间消失。通过内部缺失破坏qua-1基因功能,导致基因中部出现移码并提前终止,会导致强烈的致死性。动物由于蜕皮缺陷而在幼虫早期阶段停滞。电子显微镜显示由于蜕皮缺陷导致双层角质层,但在皮下组织中未观察到明显缺陷。仅含Qua结构域的::GFP和全长QUA-1::GFP融合构建体被分泌并与覆盖的角质层相关,但只有QUA-1::GFP能挽救突变表型。我们的结果表明,Hint/Hog结构域和Qua结构域对于QUA-1的功能都至关重要。