A Developmental Program Truncates Long Transcripts to Temporally Regulate Cell Signaling.
A Developmental Program Truncates Long Transcripts to Temporally Regulate Cell Signaling.
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发育程序截断长转录本以暂时调节细胞信号传导。
DOI:
10.1016/j.devcel.2018.11.019
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发表时间:
2018
影响因子:
11.8
通讯作者:
Stathopoulos,Angelike
中科院分区:
文献类型:
--
作者:
Sandler,JeremyE;Irizarry,Jihyun;Stepanik,Vincent;Dunipace,Leslie;Amrhein,Henry;Stathopoulos,Angelike
Rapid mitotic divisions and a fixed transcription rate limit the maximal length of transcripts in earlyDrosophilaembryos. Previous studies suggested that transcription of long genes is initiated but aborted, as early nuclear divisions have short interphases. Here, we identify long genes that are expressed during short nuclear cycles as truncated transcripts. The RNA binding protein Sex-lethal physically associates with transcripts for these genes and is required to support early termination to specify shorter transcript isoforms in early embryos of both sexes. In addition, one truncated transcript for the geneshort-gastrulationencodes a product in embryos that functionally relates to a previously characterized dominant-negative form, which maintains TGF-β signaling in the off-state. In summary, our results reveal a developmental program of short transcripts functioning to help temporally regulateDrosophilaembryonic development, keeping cell signaling at early stages to a minimum in order to support its proper initiation at cellularization.