Perrimon N, Mahowald A P
Dev Biol. 1986 Nov;118(1):28-41. doi: 10.1016/0012-1606(86)90070-9.
The maternal and zygotic effect phenotypes of mutations at the l(1)hopscotch (l(1)hop) locus are described. l(1)hop is located in 10B6-8 on the salivary gland chromosome map and 17 alleles have been characterized. A complex complementation pattern is observed among the 17 alleles. The lethal phase of null alleles of l(1)hop occurs at the larval-pupal interface associated with a small disc phenotype. Embryos produced from homozygous l(1)hop germline clones show segment specific defects. The extent of these defects depends upon both the strength of the allele and the paternal contribution. In the most extreme case embryos exhibit defects associated with five segments T2, T3, A4, A5, and A8. In the less extreme phenotype defects are only associated with A5. Thus, activity of l(1)hop+ is required both for the maintenance and continued cell division of diploid imaginal precursors and for the establishment of the full array of segments.
本文描述了位于1号染色体跳房子(l(1)hop)位点的突变所产生的母体效应和合子效应表型。l(1)hop位于唾液腺染色体图谱的10B6 - 8区域,已鉴定出17个等位基因。在这17个等位基因中观察到复杂的互补模式。l(1)hop无效等位基因的致死期出现在幼虫 - 蛹期界面,伴有小圆盘表型。由纯合l(1)hop生殖系克隆产生的胚胎表现出特定节段的缺陷。这些缺陷的程度取决于等位基因的强度和父本的贡献。在最极端的情况下,胚胎表现出与五个节段(T2、T3、A4、A5和A8)相关的缺陷。在不太极端的表型中,缺陷仅与A5相关。因此,l(1)hop+的活性对于二倍体成虫前体细胞的维持和持续细胞分裂以及完整节段阵列的建立都是必需的。