Supp D M, Brueckner M, Kuehn M R, Witte D P, Lowe L A, McGrath J, Corrales J, Potter S S
Divisions of Molecular and Developmental Biology, The Children's Hospital Research Foundation, Cincinnati, Ohio, USA.
Development. 1999 Dec;126(23):5495-504. doi: 10.1242/dev.126.23.5495.
Vertebrates develop distinct asymmetries along the left-right axis, which are consistently aligned with the anteroposterior and dorsoventral axes. The mechanisms that direct this handed development of left-right asymmetries have been elusive, but recent studies of mutations that affect left-right development have shed light on the molecules involved. One molecule implicated in left-right specification is left-right dynein (LRD), a microtubule-based motor protein. In the LRD protein of the inversus viscerum (iv) mouse, there is a single amino acid difference at a conserved position, and the lrd gene is one of many genes deleted in the legless (lgl) mutation. Both iv and lgl mice display randomized left-right development. Here we extend the analysis of the lrd gene at the levels of sequence, expression and function. The complete coding sequence of the lrd gene confirms its classification as an axonemal, or ciliary, dynein. Expression of lrd in the node at embryonic day 7.5 is shown to be symmetric. At embryonic day 8.0, however, a striking asymmetric expression pattern is observed in all three germ layers of the developing headfold, suggesting roles in both the establishment and maintenance of left-right asymmetries. At later times, expression of lrd is also observed in the developing floorplate, gut and limbs. These results suggest function for LRD protein in both ciliated and non-ciliated cells, despite its sequence classification as axonemal. In addition, a targeted mutation of lrd was generated that deletes the part of the protein required for ATP binding, and hence motor function. The resulting left-right phenotype, randomization of laterality, is identical to that of iv and lgl mutants. Gross defects in ciliary structure were not observed in lrd/lrd mutants. Strikingly, however, the monocilia on mutant embryonic node cells were immotile. These results prove the identity of the iv and lrd genes. Further, they argue that LRD motor function, and resulting nodal monocilia movement, are required for normal left-right development.
脊椎动物沿左右轴形成明显的不对称性,这些不对称性始终与前后轴和背腹轴对齐。指导左右不对称性这种特定发育的机制一直难以捉摸,但最近对影响左右发育的突变的研究揭示了其中涉及的分子。一种与左右特化有关的分子是左右动力蛋白(LRD),它是一种基于微管的驱动蛋白。在内脏逆位(iv)小鼠的LRD蛋白中,在一个保守位置有一个氨基酸差异,并且lrd基因是在无腿(lgl)突变中缺失的众多基因之一。iv和lgl小鼠都表现出左右发育随机化。在这里,我们在序列、表达和功能水平上扩展了对lrd基因的分析。lrd基因的完整编码序列证实其可归类为轴丝或纤毛动力蛋白。lrd在胚胎第7.5天的节点中的表达显示是对称的。然而,在胚胎第8.0天,在发育中的头褶的所有三个胚层中观察到明显的不对称表达模式,这表明其在左右不对称性的建立和维持中都起作用。在稍后阶段,在发育中的底板、肠道和四肢中也观察到lrd的表达。这些结果表明LRD蛋白在纤毛细胞和非纤毛细胞中都有功能,尽管其序列归类为轴丝。此外,产生了lrd的靶向突变,该突变删除了ATP结合所需的蛋白质部分,从而消除了驱动功能。由此产生的左右表型,即左右侧随机化,与iv和lgl突变体相同。在lrd/lrd突变体中未观察到纤毛结构的明显缺陷。然而,引人注目的是,突变胚胎节点细胞上的单根纤毛是不动的。这些结果证明了iv和lrd基因的一致性。此外,它们表明LRD驱动功能以及由此产生的节点单根纤毛运动是正常左右发育所必需的。