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CDK12 通过转录延伸促进表皮分化是必要的。

CDK12 Is Necessary to Promote Epidermal Differentiation Through Transcription Elongation.

机构信息

Institute of Precision Medicine, Department of Burns, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, Guangdong, China.

Department of Dermatology and Department of Cellular and Molecular Medicine, UCSD Stem Cell Program, University of California, San Diego, La Jolla, CA, USA.

出版信息

Stem Cells. 2022 Apr 29;40(4):435-445. doi: 10.1093/stmcls/sxac002.


DOI:10.1093/stmcls/sxac002
PMID:35325240
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9199850/
Abstract

Proper differentiation of the epidermis is essential to prevent water loss and to protect the body from the outside environment. Perturbations in this process can lead to a variety of skin diseases that impacts 1 in 5 people. While transcription factors that control epidermal differentiation have been well characterized, other aspects of transcription control such as elongation are poorly understood. Here we show that of the two cyclin-dependent kinases (CDK12 and CDK13), that are known to regulate transcription elongation, only CDK12 is necessary for epidermal differentiation. Depletion of CDK12 led to loss of differentiation gene expression and absence of skin barrier formation in regenerated human epidermis. CDK12 binds to genes that code for differentiation promoting transcription factors (GRHL3, KLF4, and OVOL1) and is necessary for their elongation. CDK12 is necessary for elongation by promoting Ser2 phosphorylation on the C-terminal domain of RNA polymerase II and the stabilization of binding of the elongation factor SPT6 to target genes. Our results suggest that control of transcription elongation by CDK12 plays a prominent role in adult cell fate decisions.

摘要

表皮的适当分化对于防止水分流失和保护身体免受外界环境的影响至关重要。这个过程的紊乱可能导致各种皮肤疾病,影响五分之一的人。虽然控制表皮分化的转录因子已经得到很好的描述,但转录控制的其他方面,如延伸,知之甚少。在这里,我们表明,在已知调节转录延伸的两个细胞周期蛋白依赖性激酶(CDK12 和 CDK13)中,只有 CDK12 是表皮分化所必需的。CDK12 的耗竭导致分化基因表达的丧失和再生的人类表皮中皮肤屏障形成的缺失。CDK12 与编码促进分化的转录因子(GRHL3、KLF4 和 OVOL1)的基因结合,并且是其延伸所必需的。CDK12 通过促进 RNA 聚合酶 II C 端结构域上 Ser2 的磷酸化和稳定延伸因子 SPT6 与靶基因的结合来促进延伸。我们的结果表明,CDK12 对转录延伸的控制在成体细胞命运决定中起着重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0151/9199850/f3402fd46499/sxac002_fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0151/9199850/f3402fd46499/sxac002_fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0151/9199850/f3402fd46499/sxac002_fig5.jpg

相似文献

[1]
CDK12 Is Necessary to Promote Epidermal Differentiation Through Transcription Elongation.

Stem Cells. 2022-4-29

[2]
CDK12 globally stimulates RNA polymerase II transcription elongation and carboxyl-terminal domain phosphorylation.

Nucleic Acids Res. 2020-8-20

[3]
Characterization of human cyclin-dependent kinase 12 (CDK12) and CDK13 complexes in C-terminal domain phosphorylation, gene transcription, and RNA processing.

Mol Cell Biol. 2015-3

[4]
SPT6 promotes epidermal differentiation and blockade of an intestinal-like phenotype through control of transcriptional elongation.

Nat Commun. 2021-2-4

[5]
CDK12 and Integrator-PP2A complex modulates LEO1 phosphorylation for processive transcription elongation.

Sci Adv. 2023-5-19

[6]
CDK12 is a transcription elongation-associated CTD kinase, the metazoan ortholog of yeast Ctk1.

Genes Dev. 2010-10-15

[7]
The Cyclin K/Cdk12 complex maintains genomic stability via regulation of expression of DNA damage response genes.

Genes Dev. 2011-10-15

[8]
Gene expression regulation by CDK12: a versatile kinase in cancer with functions beyond CTD phosphorylation.

Exp Mol Med. 2020-5

[9]
Discovery of 3-Benzyl-1-( trans-4-((5-cyanopyridin-2-yl)amino)cyclohexyl)-1-arylurea Derivatives as Novel and Selective Cyclin-Dependent Kinase 12 (CDK12) Inhibitors.

J Med Chem. 2018-8-20

[10]
CDK12 regulates DNA repair genes by suppressing intronic polyadenylation.

Nature. 2018-11-28

引用本文的文献

[1]
New insights into the dule roles CDK12 in human cancers: Mechanisms and interventions for cancer therapy.

J Pharm Anal. 2025-7

[2]
A lineage-specific nascent RNA assay unveils principles of gene regulation in tissue biology.

bioRxiv. 2024-10-18

本文引用的文献

[1]
Cutaneous innate immune tolerance is mediated by epigenetic control of MAP2K3 by HDAC8/9.

Sci Immunol. 2021-5-21

[2]
SPT6 promotes epidermal differentiation and blockade of an intestinal-like phenotype through control of transcriptional elongation.

Nat Commun. 2021-2-4

[3]
RAS-mediated suppression of PAR3 and its effects on SCC initiation and tissue architecture occur independently of hyperplasia.

J Cell Sci. 2020-12-7

[4]
ELL Facilitates RNA Polymerase II-Mediated Transcription of Human Epidermal Proliferation Genes.

J Invest Dermatol. 2021-5

[5]
CDK12 globally stimulates RNA polymerase II transcription elongation and carboxyl-terminal domain phosphorylation.

Nucleic Acids Res. 2020-8-20

[6]
KLF3 Mediates Epidermal Differentiation through the Epigenomic Writer CBP.

iScience. 2020-7-24

[7]
TEAD1 and TEAD3 Play Redundant Roles in the Regulation of Human Epidermal Proliferation.

J Invest Dermatol. 2020-10

[8]
BRD4 Is Necessary for Differentiation Downstream of Epidermal Lineage-Determining Transcription Factors.

J Invest Dermatol. 2020-10

[9]
Therapeutic Targeting of CDK12/CDK13 in Triple-Negative Breast Cancer.

Cancer Cell. 2019-10-24

[10]
HNRNPK maintains epidermal progenitor function through transcription of proliferation genes and degrading differentiation promoting mRNAs.

Nat Commun. 2019-9-13

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