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Analysis of haploid development based on expression patterns of developmental genes in the medaka Oryzias latipes

机译:基于Medaka Oryzias LaTipes中发育基因表达模式的单倍体开发分析

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The abnormalities of haploid medaka embryos were characterized by comparative analysis of histologic sections and expression patterns of some developmental marker genes between haploids and diploids to clarify whether medaka haploids are useful for identifying mutants. During gastrulation, an obvious defect was first observed as a delay of epiboly and involution. This delay was shown to be caused not by the perturbation of mesoderm induction, but by widespread cell death and disorganization of cell arrangement in the blastoderm. This disorganization of cell arrangement was also detected in various organs, such as the brain, somite and notochord, at a late developmental stage. Ten days after fertilization, a small head and a short body axis were formed; these changes were also observed in haploid embryos in other species, but their cause is unknown. Based on the expression patterns of HNF3beta and goosecoid, it was demonstrated that a short and impotent prechordal plate induced near the marginal zone in haploid embryos was responsible for this defect. However, in these experiments it was also demonstrated that many major organs in haploids, such as the somite and notochord, differentiated incompletely but were present. Therefore, it was concluded that haploid screening is suitable for identifying mutations revealed by an obvious phenotype, such as dorsoventral polarity.
机译:通过对单倍体和二倍体之间的一些发育标记基因的组织区切片和表达模式的比较分析来表征单倍体MedaKa胚胎的异常,以阐明Medaka Haploids是否可用于鉴定突变体是有用的。在腐殖过程中,首先观察到明显的缺陷作为表皮和联系的延迟。显示这种延迟不是由中胚层诱导的扰动引起的,而是通过胚乳中的广泛细胞死亡和细胞排列的紊乱。在延迟发育阶段,还在各种器官中检测到细胞布置的这种细胞排列的紊乱。施肥后十天,形成小头和短体轴;在其他物种的单倍体胚胎中也观察到这些变化,但它们的原因是未知的。基于HNF3β和毒素的表达模式,证明了单倍体胚胎边缘区附近诱导的短且无能的细胞板对该缺陷负责。然而,在这些实验中,还证明了单倍体中的许多主要器官,例如SOMITE和NOCOCOLOR,分化不完全但存在。因此,结论是,单倍体筛选适用于鉴定由明显表型的突变,例如背络极性。

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