Horne-Badovinac S, Lin D, Waldron S, Schwarz M, Mbamalu G, Pawson T, Jan Y, Stainier D Y, Abdelilah-Seyfried S
Departments of Biochemistry and Biophysics, Programs in Developmental Biology, Genetics and Human Genetics, University of California-San Francisco, 94143, San Francisco, CA, USA
Curr Biol. 2001 Oct 2;11(19):1492-502. doi: 10.1016/s0960-9822(01)00458-4.
The Par-3/Par-6/aPKC complex is a key regulator of cell polarity in a number of systems. In Drosophila, this complex acts at the zonula adherens (adherens junctions) to establish epithelial polarity and helps to orient the mitotic spindle during asymmetric neuroblast divisions. In MDCKII cells, this complex localizes to the zonula occludens (tight junctions) and appears to regulate epithelial polarity. However, the in vivo role of this complex during vertebrate embryogenesis is not known, due to the lack of relevant mutations.
We have positionally cloned the zebrafish heart and soul (has) mutation, which affects the morphogenesis of several embryonic tissues, and show that it encodes atypical protein kinase C lambda (aPKC lambda). We find that loss of aPKC lambda affects the formation and maintenance of the zonula adherens in the polarized epithelia of the retina, neural tube, and digestive tract, leading to novel phenotypes, such as the formation of multiple lumens in the developing intestine. In addition, has mutants display defects in gut looping and endodermal organ morphogenesis that appear to be independent of the defects in epithelial polarity. Finally, we show that loss of aPKC lambda leads to defects in spindle orientation during progenitor cell divisions in the neural retina.
Our results show that aPKC lambda is required for the formation and maintenance of the zonula adherens during early epithelial development in vertebrates and demonstrate a previously undescribed yet critical role for this protein in organ morphogenesis. Furthermore, our studies identify the first genetic locus regulating the orientation of cell division in vertebrates.
Par-3/Par-6/aPKC复合物是多个系统中细胞极性的关键调节因子。在果蝇中,该复合物作用于黏着连接以建立上皮极性,并在不对称神经母细胞分裂过程中帮助定向有丝分裂纺锤体。在MDCKII细胞中,该复合物定位于紧密连接,似乎调节上皮极性。然而,由于缺乏相关突变,该复合物在脊椎动物胚胎发育过程中的体内作用尚不清楚。
我们通过定位克隆了斑马鱼“心灵”(heart and soul,has)突变体,该突变影响多个胚胎组织的形态发生,并表明它编码非典型蛋白激酶Cλ(aPKCλ)。我们发现aPKCλ的缺失影响视网膜、神经管和消化道极化上皮中黏着连接的形成和维持,导致新的表型,如发育中的肠道形成多个管腔。此外,has突变体在肠道环化和内胚层器官形态发生方面表现出缺陷,这些缺陷似乎与上皮极性缺陷无关。最后我们表明,aPKCλ的缺失导致神经视网膜祖细胞分裂过程中纺锤体定向缺陷。
我们的结果表明,aPKCλ是脊椎动物早期上皮发育过程中黏着连接形成和维持所必需的,并证明了该蛋白在器官形态发生中一个以前未描述但至关重要的作用。此外,我们的研究确定了第一个调节脊椎动物细胞分裂方向的基因位点。