4.4 Article

Forward genetics identifies Kdf1/1810019J16Rik as an essential regulator of the proliferation-differentiation decision in epidermal progenitor cells

期刊

DEVELOPMENTAL BIOLOGY
卷 383, 期 2, 页码 201-213

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ydbio.2013.09.022

关键词

Progenitor cells; Epidermis; Development; Keratinocyte; Cell fate decision; Mouse; Forward genetics

资金

  1. NIAMS NIH HHS [R01 AR059687, R0AR059687] Funding Source: Medline
  2. NICHD NIH HHS [R01HD32427, R01 HD032427, U01 HD043478] Funding Source: Medline
  3. NINDS NIH HHS [R01NS044385, R01 NS044385] Funding Source: Medline

向作者/读者索取更多资源

Cell fate decisions during embryogenesis and adult life govern tissue formation, homeostasis and repair. Two key decisions that must be tightly coordinated are proliferation and differentiation. Overproliferation can lead to hyperplasia or tumor formation while premature differentiation can result in a depletion of proliferating cells and organ failure. Maintaining this balance is especially important in tissues that undergo rapid turnover like skin however, despite recent advances, the genetic mechanisms that balance cell differentiation and proliferation are still unclear. In an unbiased genetic screen to identify genes affecting early development, we identified an essential regulator of the proliferation-differentiation balance in epidermal progenitor cells, the Keratinocyte differentiation factor 1 (Kdfl; 1810019J16Rik) gene. Kdfl is expressed in epidermal cells from early stages of epidermis formation through adulthood. Specifically, Kdfl is expressed both in epidermal progenitor cells where it acts to curb the rate of proliferation as well as in their progeny where it is required to block proliferation and promote differentiation. Consequently, Kdf1 mutants display both uncontrolled cell proliferation in the epidermis and failure to develop terminal fates. Our findings reveal a dual role for the novel gene Kdfl both as a repressive signal for progenitor cell proliferation through its inhibition of p63 and a strong inductive signal for terminal differentiation through its interaction with the cell cycle regulator Stratifin. (C) 2013 Elsevier Inc. All rights reserved.

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