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Norway

PMID:22570637  

YY1 regulates melanocyte development and function by cooperating with MITF.

Juying Li | Jun S Song | Robert J A Bell | Thanh-Nga T Tran | Rizwan Haq | Huifei Liu | Kevin T Love | Robert Langer | Daniel G Anderson | Lionel Larue | David E Fisher
PLoS genetics | 2012

Studies of coat color mutants have greatly contributed to the discovery of genes that regulate melanocyte development and function. Here, we generated Yy1 conditional knockout mice in the melanocyte-lineage and observed profound melanocyte deficiency and premature gray hair, similar to the loss of melanocytes in human piebaldism and Waardenburg syndrome. Although YY1 is a ubiquitous transcription factor, YY1 interacts with M-MITF, the Waardenburg Syndrome IIA gene and a master transcriptional regulator of melanocytes. YY1 cooperates with M-MITF in regulating the expression of piebaldism gene KIT and multiple additional pigmentation genes. Moreover, ChIP-seq identified genome-wide YY1 targets in the melanocyte lineage. These studies mechanistically link genes implicated in human conditions of melanocyte deficiency and reveal how a ubiquitous factor (YY1) gains lineage-specific functions by co-regulating gene expression with a lineage-restricted factor (M-MITF)-a general mechanism which may confer tissue-specific gene expression in multiple lineages.

Pubmed ID: 22570637

Research resources used in this publication

None found

Antibodies used in this publication

None found

Associated grants

  • Agency: NIBIB NIH HHS, United States
    Id: R01 EB000244
  • Agency: NIAMS NIH HHS, United States
    Id: T32 AR007098
  • Agency: NCI NIH HHS, United States
    Id: R01 CA163336
  • Agency: NIAMS NIH HHS, United States
    Id: R01 AR043369
  • Agency: NCI NIH HHS, United States
    Id: R01CA163336
  • Agency: NIAMS NIH HHS, United States
    Id: 2T32AR007098-37
  • Agency: NIGMS NIH HHS, United States
    Id: T32 GM008568
  • Agency: NIBIB NIH HHS, United States
    Id: R37 EB000244

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