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叉头转录因子在涡虫中线上被诱导产生,对于前端再生是必需的。

A forkhead transcription factor is wound-induced at the planarian midline and required for anterior pole regeneration.

机构信息

Howard Hughes Medical Institute, MIT Biology and Whitehead Institute for Biomedical Research, Cambridge, Massachusetts, United States of America.

出版信息

PLoS Genet. 2014 Jan;10(1):e1003999. doi: 10.1371/journal.pgen.1003999. Epub 2014 Jan 9.

Abstract

Planarian regeneration requires positional information to specify the identity of tissues to be replaced as well as pluripotent neoblasts capable of differentiating into new cell types. We found that wounding elicits rapid expression of a gene encoding a Forkhead-family transcription factor, FoxD. Wound-induced FoxD expression is specific to the ventral midline, is regulated by Hedgehog signaling, and is neoblast-independent. FoxD is subsequently expressed within a medial subpopulation of neoblasts at wounds involving head regeneration. Ultimately, FoxD is co-expressed with multiple anterior markers at the anterior pole. Inhibition of FoxD with RNA interference (RNAi) results in the failure to specify neoblasts expressing anterior markers (notum and prep) and in anterior pole formation defects. FoxD(RNAi) animals fail to regenerate a new midline and to properly pattern the anterior blastema, consistent with a role for the anterior pole in organizing pattern of the regenerating head. Our results suggest that wound signaling activates a forkhead transcription factor at the midline and, if the head is absent, FoxD promotes specification of neoblasts at the prior midline for anterior pole regeneration.

摘要

涡虫再生需要位置信息来指定要替换的组织的身份,以及能够分化为新细胞类型的多能性成体干细胞。我们发现,创伤会引发编码 Forkhead 家族转录因子 FoxD 的基因的快速表达。伤口诱导的 FoxD 表达特异性位于腹中线,受 Hedgehog 信号通路调控,与成体干细胞无关。FoxD 随后在涉及头部再生的伤口中位于成体干细胞的内侧亚群中表达。最终,FoxD 与前极的多个前体标记物共同表达。使用 RNA 干扰 (RNAi) 抑制 FoxD 会导致表达前体标记物(notum 和 prep)的成体干细胞无法特化,并导致前极形成缺陷。FoxD(RNAi) 动物无法再生新的中线,也无法正确形成前芽体,这与前极在头部再生中组织模式的作用一致。我们的结果表明,创伤信号在中线激活叉头转录因子,如果头部缺失,FoxD 会促进前中线成体干细胞的特化,用于前极再生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0694/3886891/3f848eba8978/pgen.1003999.g001.jpg

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