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果蝇黑腹背侧组基因 fs(1)原肠胚形成缺陷的发育分析。

Developmental analysis of fs(1)gastrulation defective, a dorsal-group gene of Drosophila melanogaster.

作者信息

Konrad Kenneth D, Goralski Thomas J, Mahowald Anthony P

机构信息

Department of Developmental Genetics and Anatomy, Case Western Reserve University, School of Medicine, 44106, Cleveland, Ohio, USA.

出版信息

Rouxs Arch Dev Biol. 1988 Mar;197(2):75-91. doi: 10.1007/BF00375930.

Abstract

The gastrulation defective (gd) locus is a maternally expressed gene in Drosophila required for normal differentiation of structures along the embryonic dorso-ventral axis. Cuticular defects of the offspring from females with different combinations of gd alleles comprised a phenotypic continuum. Complementation among several alleles produced normal offspring while progressively more severe mutations produced a graded loss of structures from ventral, and then lateral, blastoderm cells. The most severely affected embryos consisted entirely of structures derived from dorsal blastoderm cells. Histological examination of staged siblings from selected allelic combinations showed that internal tissues were similarly affected. The tissues observed in amorphic embryos support new, more dorsal, assignments of fate map positions for blastoderm precursors of the cephalopharyngeal apparatus, hindgut and ventral nerve cord. The loss of ventral and lateral structures did not occur through cell death and appeared to involve a change in blastoderm cell fate. A direct effect of the mutations on blastoderm cell determination, however, was insufficient to explain the development of the dorsalized embryos. Intermediate phenotypes suggested that cell interactions or movements associated with morphogenesis are required for the determination of some cell fates in the dorsoventral axis. Thus, the developmental fate of all blastoderm cells may not be fixed at the time of blastoderm formation.

摘要

原肠胚形成缺陷(gd)基因座是果蝇中一个由母体表达的基因,对于沿胚胎背腹轴的结构正常分化是必需的。具有不同gd等位基因组合的雌性后代的表皮缺陷构成了一个表型连续体。几个等位基因之间的互补产生了正常的后代,而逐渐更严重的突变则导致腹侧,然后是侧部胚盘细胞结构逐渐丧失。受影响最严重的胚胎完全由源自背侧胚盘细胞的结构组成。对选定等位基因组合的分期同胞进行组织学检查表明,内部组织也受到类似影响。在无义胚胎中观察到的组织支持对头部咽器官、后肠和腹神经索的胚盘前体的命运图位置进行新的、更偏向背侧的定位。腹侧和侧部结构的丧失不是通过细胞死亡发生的,似乎涉及胚盘细胞命运的改变。然而,突变对胚盘细胞决定的直接影响不足以解释背化胚胎的发育。中间表型表明,形态发生相关的细胞相互作用或运动对于背腹轴上某些细胞命运的决定是必需的。因此,所有胚盘细胞的发育命运可能在胚盘形成时并未固定。

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