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促进斑马鱼轴中胚层的脊索命运并抑制肌肉发育。

Promoting notochord fate and repressing muscle development in zebrafish axial mesoderm.

作者信息

Amacher S L, Kimmel C B

机构信息

Institute of Neuroscience, University of Oregon, Eugene, OR 97403-1254, USA.

出版信息

Development. 1998 Apr;125(8):1397-406. doi: 10.1242/dev.125.8.1397.

Abstract

Cell fate decisions in early embryonic cells are controlled by interactions among developmental regulatory genes. Zebrafish floating head mutants lack a notochord; instead, muscle forms under the neural tube. As shown previously, axial mesoderm in floating head mutant gastrulae fails to maintain expression of notochord genes and instead expresses muscle genes. Zebrafish spadetail mutant gastrulae have a nearly opposite phenotype; notochord markers are expressed in a wider domain than in wild-type embryos and muscle marker expression is absent. We examined whether these two phenotypes revealed an antagonistic genetic interaction by constructing the double mutant. Muscle does not form in the spadetail;floating head double mutant midline, indicating that spadetail function is required for floating head mutant axial mesoderm to transfate to muscle. Instead, the midline of spadetail;floating head double mutants is greatly restored compared to that of floating head mutants; the floor plate is almost complete and an anterior notochord develops. In addition, we find that floating head mutant cells can make both anterior and posterior notochord when transplanted into a wild-type host, showing that enviromental signals can override the predisposition of floating head mutant midline cells to make muscle. Taken together, these results suggest that repression of spadetail function by floating head is critical to promote notochord fate and prevent midline muscle development, and that cells can be recruited to the notochord by environmental signals.

摘要

早期胚胎细胞中的细胞命运决定受发育调控基因之间的相互作用控制。斑马鱼浮头突变体缺乏脊索;取而代之的是,肌肉在神经管下方形成。如先前所示,浮头突变体原肠胚中的轴向中胚层无法维持脊索基因的表达,而是表达肌肉基因。斑马鱼短尾突变体原肠胚具有几乎相反的表型;与野生型胚胎相比,脊索标记物在更广泛的区域表达,且不存在肌肉标记物表达。我们通过构建双突变体来研究这两种表型是否揭示了一种拮抗遗传相互作用。在短尾;浮头双突变体的中线处不形成肌肉,这表明浮头突变体轴向中胚层转变为肌肉需要短尾功能。相反,与浮头突变体相比,短尾;浮头双突变体的中线得到了极大恢复;底板几乎完整,并且发育出了前部脊索。此外,我们发现,当将浮头突变体细胞移植到野生型宿主中时,它们可以形成前部和后部脊索,这表明环境信号可以克服浮头突变体中线细胞形成肌肉的倾向。综上所述,这些结果表明,浮头对短尾功能的抑制对于促进脊索命运和防止中线肌肉发育至关重要,并且细胞可以被环境信号募集到脊索中。

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