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同源域蛋白 Six4 防止果蝇多余 II 型神经母细胞的产生和中间神经祖细胞的过早分化。

Homeodomain protein Six4 prevents the generation of supernumerary Drosophila type II neuroblasts and premature differentiation of intermediate neural progenitors.

机构信息

Department of Neuroscience and Physiology, State University of New York Upstate Medical University, Syracuse, New York, United States of America.

出版信息

PLoS Genet. 2021 Feb 8;17(2):e1009371. doi: 10.1371/journal.pgen.1009371. eCollection 2021 Feb.

DOI:10.1371/journal.pgen.1009371
PMID:33556050
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7895384/
Abstract

In order to boost the number and diversity of neurons generated from neural stem cells, intermediate neural progenitors (INPs) need to maintain their homeostasis by avoiding both dedifferentiation and premature differentiation. Elucidating how INPs maintain homeostasis is critical for understanding the generation of brain complexity and various neurological diseases resulting from defects in INP development. Here we report that Six4 expressed in Drosophila type II neuroblast (NB) lineages prevents the generation of supernumerary type II NBs and premature differentiation of INPs. We show that loss of Six4 leads to supernumerary type II NBs likely due to dedifferentiation of immature INPs (imINPs). We provide data to further demonstrate that Six4 inhibits the expression and activity of PntP1 in imINPs in part by forming a trimeric complex with Earmuff and PntP1. Furthermore, knockdown of Six4 exacerbates the loss of INPs resulting from the loss of PntP1 by enhancing ectopic Prospero expression in imINPs, suggesting that Six4 is also required for preventing premature differentiation of INPs. Taken together, our work identified a novel transcription factor that likely plays important roles in maintaining INP homeostasis.

摘要

为了促进神经干细胞产生更多样化的神经元,中间神经祖细胞(INP)需要通过避免去分化和过早分化来维持其体内平衡。阐明 INP 如何维持体内平衡对于理解大脑复杂性的产生以及由于 INP 发育缺陷导致的各种神经疾病至关重要。在这里,我们报告在果蝇 II 型神经母细胞(NB)谱系中表达的 Six4 可防止多余的 II 型 NB 的产生和 INP 的过早分化。我们表明,Six4 的缺失可能会导致多余的 II 型 NB,这是由于不成熟的 INP(imINP)去分化引起的。我们提供的数据进一步证明,Six4 通过与 Earmuff 和 PntP1 形成三聚体复合物,部分抑制 imINP 中 PntP1 的表达和活性。此外,Six4 的敲低通过增强 imINP 中异位 Prospero 的表达,加剧了 PntP1 缺失导致的 INP 缺失,这表明 Six4 也需要防止 INP 的过早分化。总之,我们的工作确定了一种新型转录因子,它可能在维持 INP 体内平衡方面发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a78/7895384/33ceb41c5919/pgen.1009371.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a78/7895384/202222e9d974/pgen.1009371.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a78/7895384/d7d4b078efcb/pgen.1009371.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a78/7895384/f608adf57767/pgen.1009371.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a78/7895384/88164f533c80/pgen.1009371.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a78/7895384/94482aa12ce7/pgen.1009371.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a78/7895384/bf5ca7c4f1dc/pgen.1009371.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a78/7895384/33ceb41c5919/pgen.1009371.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a78/7895384/202222e9d974/pgen.1009371.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a78/7895384/d7d4b078efcb/pgen.1009371.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a78/7895384/f608adf57767/pgen.1009371.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a78/7895384/88164f533c80/pgen.1009371.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a78/7895384/94482aa12ce7/pgen.1009371.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a78/7895384/bf5ca7c4f1dc/pgen.1009371.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a78/7895384/33ceb41c5919/pgen.1009371.g007.jpg

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