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The C. elegans tailless/Tlx homolog nhr-67 regulates a stage-specific program of linker cell migration in male gonadogenesis

机译:秀丽隐杆线虫无尾/ Tlx同源物nhr-67调节雄性生殖腺发生中连接细胞迁移的特定阶段程序。

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摘要

Cell migration is a common event during organogenesis, yet little is known about how migration is temporally coordinated with organ development. We are investigating stage-specific programs of cell migration using the linker cell (LC), a migratory cell crucial for male gonadogenesis of C. elegans. During the L3 and L4 larval stages of wild-type males, the LC undergoes changes in its position along the migratory route, in transcriptional regulation of the unc-5 netrin receptor and zmp-1 zinc matrix metalloprotease, and in cell morphology. We have identified the tailless homolog nhr-67 as a cell-autonomous, stage-specific regulator of timing in LC migration programs. In nhr-67-deficient animals, each of the L3 and L4 stage changes is either severely delayed or never occurs, yet LC development before the early L3 stage or after the mid-L4 stage occurs with normal timing. We propose that there is a basal migration program utilized throughout LC migration that is modified by stage-specific regulators such as nhr-67.
机译:细胞迁移是器官发生期间的常见事件,但对于迁移如何在时间上与器官发育协调知之甚少。我们正在研究使用连接细胞(LC)的阶段特定程序,该程序是对秀丽隐杆线虫的雄性腺发生至关重要的迁移细胞。在野生型雄性的L3和L4幼虫阶段,LC沿迁移途径发生位置变化,对unc-5 netrin受体和zmp-1锌基质金属蛋白酶进行转录调节,并在细胞形态上发生变化。我们已将无尾同源物nhr-67确定为LC迁移程序中的细胞自主,阶段特定的时序调节器。在nhr-67缺乏的动物中,L3和L4阶段的变化要么被严重延迟,要么从未发生,但L3早期之前或L4中期之后的LC发育按正常时机发生。我们建议在整个LC迁移过程中使用一个基础迁移程序,该程序由特定于阶段的监管机构(例如nhr-67)进行了修改。

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