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分析 NSD3 依赖性神经嵴基因表达揭示了已知和新的候选调控因子。

Profiling NSD3-dependent neural crest gene expression reveals known and novel candidate regulatory factors.

机构信息

Department of Biology, Hamline University, MS-B1807, 1536 Hewitt Ave, St Paul, MN, 55104, USA.

Department of Genetics, Cell Biology and Development, University of Minnesota, 6-160 Jackson Hall, 321 Church St SE, Minneapolis, MN, 55455, USA; Developmental Biology Center, University of Minnesota, 6-160 Jackson Hall, 321 Church St SE, Minneapolis, MN, 55455, USA.

出版信息

Dev Biol. 2021 Jul;475:118-130. doi: 10.1016/j.ydbio.2021.02.015. Epub 2021 Mar 8.

DOI:10.1016/j.ydbio.2021.02.015
PMID:33705737
Abstract

The lysine methyltransferase NSD3 is required for the expression of key neural crest transcription factors and the migration of neural crest cells. Nevertheless, a complete view of the genes dependent upon NSD3 for expression and the developmental processes impacted by NSD3 in the neural crest was lacking. We used RNA sequencing (RNA-seq) to profile transcripts differentially expressed after NSD3 knockdown in chick premigratory neural crest cells, identifying 674 genes. Gene Ontology and gene set enrichment analyses further support a requirement for NSD3 during neural crest development and show that NSD3 knockdown also upregulates ribosome biogenesis. To validate our results, we selected three genes not previously associated with neural crest development, Astrotactin 1 (Astn1), Dispatched 3 (Disp3), and Tropomyosin 1 (Tpm1). Using whole mount in situ hybridization, we show that premigratory neural crest cells express these genes and that NSD3 knockdown downregulates (Astn1 and Disp3) and upregulates (Tpm1) their expression, consistent with RNA-seq results. Altogether, this study identifies novel putative regulators of neural crest development and provides insight into the transcriptional consequences of NSD3 in the neural crest, with implications for cancer.

摘要

赖氨酸甲基转移酶 NSD3 对于关键神经嵴转录因子的表达和神经嵴细胞的迁移是必需的。然而,对于依赖 NSD3 表达的基因以及 NSD3 在神经嵴中影响的发育过程,我们还没有一个完整的认识。我们使用 RNA 测序(RNA-seq)来分析 NSD3 在鸡前迁移神经嵴细胞中敲低后的差异表达转录本,鉴定出 674 个基因。基因本体论和基因集富集分析进一步支持 NSD3 在神经嵴发育过程中的必要性,并表明 NSD3 敲低也上调了核糖体生物发生。为了验证我们的结果,我们选择了三个以前与神经嵴发育无关的基因,Astrotactin 1(Astn1)、Dispatched 3(Disp3)和 Tropomyosin 1(Tpm1)。通过全胚胎原位杂交,我们表明前迁移神经嵴细胞表达这些基因,而 NSD3 敲低下调(Astn1 和 Disp3)和上调(Tpm1)它们的表达,与 RNA-seq 结果一致。总之,这项研究鉴定了神经嵴发育的新的潜在调节因子,并深入了解了 NSD3 在神经嵴中的转录后果,这对癌症具有重要意义。

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