White K, DeCelles N L, Enlow T C
Genetics. 1983 Jul;104(3):433-48. doi: 10.1093/genetics/104.3.433.
Genetic and developmental analysis of an X-linked vital locus vnd was undertaken. Embryos hemizygous for the original allele vnd did not hatch and exhibited a disorganized ventral nervous system (VNS). The mutation maps in the region 1B6-7 to 1B9-10, a subregion of an area previously shown to be essential to normal neural development. In this paper, we report isolation of five new alleles at the locus vnd. Genetic complementation analysis of all mutations at the vnd locus, with lethal alleles at adjacent loci, indicates that all lesions at the locus vnd affect only one vital gene function in the region. Four of the five alleles are embryonic lethal; one allele is subvital and behaves like an hypomorphic mutation. Hemizygous embryos for three of the four embryonic lethal alleles were inspected in histological sections; all exhibited disorganized VNS similar to the original allele. The developmental analysis in gynandromorphic genetic mosaics shows that (1) vnd+ gene function is not essential in most imaginal-disc cell derivatives, (2) only about 30% of the mosaic zygotes survive as adults, (3) mosaic zygotes with mutant tissue close to the head cuticle are least likely to survive, and (4) mutant tissue in the thoracic ganglion in the adult is not necessarily lethal. The mosaic data are consistent with the vnd+ gene function being necessary in neural cells derived from the anterioventral region of the blastoderm.
对一个X连锁的重要基因座vnd进行了遗传和发育分析。原始等位基因vnd的半合子胚胎无法孵化,并表现出腹侧神经系统(VNS)紊乱。该突变定位于1B6 - 7至1B9 - 10区域,这是先前已证明对正常神经发育至关重要的一个区域的子区域。在本文中,我们报告了在vnd基因座分离出五个新的等位基因。vnd基因座所有突变与相邻基因座的致死等位基因的遗传互补分析表明,vnd基因座的所有损伤仅影响该区域的一个重要基因功能。五个等位基因中有四个是胚胎致死的;一个等位基因是亚致死的,表现为次等位基因突变。对四个胚胎致死等位基因中的三个的半合子胚胎进行了组织学切片检查;所有胚胎都表现出与原始等位基因相似的VNS紊乱。在雌雄嵌合体遗传嵌合体中的发育分析表明:(1)vnd +基因功能在大多数成虫盘细胞衍生物中并非必需;(2)只有约30%的嵌合受精卵能发育为成虫;(3)头部角质层附近有突变组织的嵌合受精卵存活可能性最小;(4)成虫胸神经节中的突变组织不一定是致死的。这些嵌合体数据与vnd +基因功能在胚盘前腹侧区域衍生的神经细胞中是必需的这一观点一致。