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发育中鼠脑 DCLK1 异构体的时空多样性。

Spatial and temporal diversity of DCLK1 isoforms in developing mouse brain.

机构信息

Department of Biological Sciences, Graduate School of Science, Japan.

Department of Biological Sciences, Graduate School of Science, Japan.

出版信息

Neurosci Res. 2021 Sep;170:154-165. doi: 10.1016/j.neures.2020.12.004. Epub 2021 Jan 22.

Abstract

Doublecortin-like kinase 1 (DCLK1) is a Doublecortin family kinase involved in a range of brain development processes including cell migration, axon/dendrite growth, and synapse development. The Dclk1 gene potentially generates multiple splicing isoforms, but the detailed expression patterns in the brain as well as in vivo functions of each isoform are still incompletely understood. Here we assessed expression patterns of DCLK1 isoforms using multiple platforms including in silico, in situ, and in vitro datasets in the developing mouse brain, and show quantitative evidence that among the four DCLK1 isoforms, DCLK1-L and DCL are mainly expressed in the embryonic cortex whereas DCLK1-L and CPG16 become dominant compared to DCL and CARP in the postnatal cortex. We also provide compelling evidence that DCLK1 isoforms are distributed in the partially distinct brain regions in the embryonic and the postnatal stages. We further show that overexpression of DCLK1-L, but not the other isoforms, in neural progenitors causes severe migration defects in the cortex, and that the migration defects are dependent on the kinase activity of DCLK1-L. Our data thus uncover partially segregated localization of DCLK1 isoforms in the developing mouse brain and suggest different roles for distinct DCLK1 isoforms in the brain development and function.

摘要

双皮质素样激酶 1(DCLK1)是双皮质素家族激酶,参与多种脑发育过程,包括细胞迁移、轴突/树突生长和突触发育。Dclk1 基因可能产生多种剪接异构体,但每种异构体在脑中的详细表达模式以及体内功能仍不完全清楚。在这里,我们使用包括在体、原位和体外数据集在内的多种平台评估了发育中小鼠脑中 DCLK1 异构体的表达模式,并提供了定量证据表明,在四种 DCLK1 异构体中,DCLK1-L 和 DCL 主要在胚胎皮层中表达,而 DCLK1-L 和 CPG16 在出生后皮层中比 DCL 和 CARP 更占优势。我们还提供了令人信服的证据表明,DCLK1 异构体在胚胎和出生后的阶段分布在部分不同的脑区。我们进一步表明,在神经前体细胞中过表达 DCLK1-L,但不是其他异构体,会导致皮层严重的迁移缺陷,并且这种迁移缺陷依赖于 DCLK1-L 的激酶活性。我们的数据因此揭示了 DCLK1 异构体在发育中小鼠脑中的部分分离定位,并表明不同的 DCLK1 异构体在大脑发育和功能中具有不同的作用。

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