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

被引:10
作者
Jacques-Fricke, Bridget T. [1 ]
Roffers-Agarwal, Julaine [2 ,3 ]
Hussein, Amina O. [2 ,4 ]
Yoder, Kendra J. [1 ]
Gearhart, Micah D. [2 ,3 ]
Gammill, Laura S. [2 ,3 ]
机构
[1] Hamline Univ, Dept Biol, MS-B1807,1536 Hewitt Ave, St Paul, MN 55104 USA
[2] Univ Minnesota, Dept Genet Cell Biol & Dev, 6-160 Jackson Hall,321 Church St SE, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Dev Biol Ctr, 6-160 Jackson Hall,321 Church St SE, Minneapolis, MN 55455 USA
[4] Univ Calif Irvine, Ctr Complex Biol Syst, 2634 Biol Sci 3, Irvine, CA 92697 USA
基金
美国国家科学基金会;
关键词
Neural crest; NSD3; RNA-Sequencing; Astrotactin; 1; Dispatched; 3; Tropomyosin; RIBOSOME BIOGENESIS; HISTONE H3; TRANSCRIPTION; NETWORK; PROTEIN; CANCER; ASTROTACTIN; MIGRATION; PROMOTES; CELLS;
D O I
10.1016/j.ydbio.2021.02.015
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:118 / 130
页数:13
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