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Lin28/let-7 通路调控哺乳动物尾部躯体延伸程序。

The Lin28/let-7 Pathway Regulates the Mammalian Caudal Body Axis Elongation Program.

机构信息

Division of Pediatric Hematology/Oncology, Children's Hospital Boston, Boston, MA 02115, USA; Howard Hughes Medical Institute, Boston, MA 02115, USA; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA; Harvard Stem Cell Institute, Boston, MA 02115, USA.

Harvard Stem Cell Institute, Boston, MA 02115, USA; Department of Pathology, Brigham and Women's Hospital, Boston, MA 02115, USA; Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Dev Cell. 2019 Feb 11;48(3):396-405.e3. doi: 10.1016/j.devcel.2018.12.016. Epub 2019 Jan 17.

Abstract

The heterochronic genes Lin28a/b and let-7 regulate invertebrate development, but their functions in patterning the mammalian body plan remain unexplored. Here, we describe how Lin28/let-7 influence caudal vertebrae number during body axis formation. We found that FoxD1-driven overexpression of Lin28a strikingly increased caudal vertebrae number and tail bud cell proliferation, whereas its knockout did the opposite. Lin28a overexpression downregulated the neural marker Sox2, causing a pro-mesodermal phenotype with a decreased proportion of neural tissue relative to nascent mesoderm. Manipulating Lin28a and let-7 led to opposite effects, and manipulating Lin28a's paralog, LIN28B caused similar yet distinct phenotypes. These findings suggest that Lin28/let-7 play a role in the regulation of tail length through heterochrony of the body plan. We propose that the Lin28/let-7 pathway controls the pool of caudal progenitors during tail development, promoting their self-renewal and balancing neural versus mesodermal cell fate decisions.

摘要

Lin28a/b 和 let-7 等异型基因调控无脊椎动物发育,但它们在塑造哺乳动物体型方面的功能仍未被探索。本文描述了 Lin28/let-7 在体轴形成过程中如何影响尾部椎体的数量。研究发现,FoxD1 驱动的 Lin28a 过表达可显著增加尾部椎体数量和尾部芽细胞增殖,而 Lin28a 敲除则相反。Lin28a 过表达下调神经标志物 Sox2,导致具有减少的神经组织相对于新兴中胚层的比例的促中胚层表型。操纵 Lin28a 和 let-7 导致相反的效果,而操纵 Lin28a 的同源物 LIN28B 则导致类似但不同的表型。这些发现表明,Lin28/let-7 通过体型的异时性在调节尾部长度方面发挥作用。研究提出,Lin28/let-7 通路在尾部发育过程中控制尾部祖细胞的库,促进它们的自我更新,并平衡神经与中胚层细胞命运的决定。

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