Mathe E, Boros I, Josvay K, Li K, Puro J, Kaufman T C, Szabad J
Department of Biology, Albert Szent-Györgyi Medical University, Szeged, Hungary.
J Cell Sci. 1998 Apr;111 ( Pt 7):887-96. doi: 10.1242/jcs.111.7.887.
The three dominant TomajD and their eleven revertant (TomajR) alleles have been localized to the alpha Tubulin67C gene of Drosophila melanogaster. Although the meiotic divisions are normally completed in eggs laid by TomajD/+, TomajD/-, TomajR/- females, embryogenesis arrests prior to the gonomeric division. The arrest is caused by: (1) the failure of prominent sperm aster formation; and (2) a consequent lack of female pronuclear migration towards the male pronucleus. Concomitant with the sperm aster defect, the four female meiotic products fuse (tetra-fusion), similar to what is seen in eggs of wild-type virgin females. In eggs of females heterozygous for weaker TomajR alleles, embryogenesis comes to a cessation before or shortly after cortical migration of cleavage nuclei. The apparent source of embryonic defect is the cleavage spindle apparatus. One of the three TomajD alleles is cold-sensitive and its cold-sensitive period coincides with the completion of female meiosis and pronuclear migration. Disorganized central and peripheral nervous systems are also characteristic of embryos derived from the temperature-sensitive TomajD/+ females. The Tomaj mutant phenotypes indicate an involvement of the normal alpha Tubulin67C gene product in: (1) the formation of the sperm aster; (2) cleavage spindle apparatus formation/function; and (3) the differentiation of the embryonic nervous system. The TomajD alleles encode a normal-sized alpha Tubulin67C isotype. Sequence analyses of the TomajD alleles revealed the replacement in different positions of a single negatively charged or neutral amino acid with a positively charged one. These residues presumably identify important functional sites.
三种主要的TomajD及其11种回复体(TomajR)等位基因已定位到黑腹果蝇的α微管蛋白67C基因上。尽管减数分裂通常在TomajD / +、TomajD / -、TomajR / -雌性所产的卵中完成,但胚胎发生在合胞体分裂之前就停止了。这种停滞是由以下原因引起的:(1)显著的精子星体形成失败;(2)随之而来的雌性原核向雄性原核迁移的缺乏。与精子星体缺陷同时发生的是,四个雌性减数分裂产物融合(四倍融合),这与野生型处女雌果蝇的卵中所见情况类似。在较弱的TomajR等位基因杂合的雌性的卵中,胚胎发生在卵裂核的皮层迁移之前或之后不久就停止了。胚胎缺陷的明显来源是卵裂纺锤体装置。三种TomajD等位基因之一对温度敏感,其温度敏感期与雌性减数分裂和原核迁移的完成相吻合。来自温度敏感的TomajD / +雌性的胚胎也具有中枢和外周神经系统紊乱的特征。Tomaj突变体表型表明正常的α微管蛋白67C基因产物参与了:(1)精子星体的形成;(2)卵裂纺锤体装置的形成/功能;(3)胚胎神经系统的分化。TomajD等位基因编码一种正常大小的α微管蛋白67C同种型。对TomajD等位基因的序列分析显示,在不同位置上,单个带负电荷或中性的氨基酸被带正电荷的氨基酸所取代。这些残基大概确定了重要的功能位点。