Literature DB >> 33468999

Interplay between cofactors and transcription factors in hematopoiesis and hematological malignancies.

Zi Wang1,2, Pan Wang3, Yanan Li3, Hongling Peng4, Yu Zhu3, Narla Mohandas5, Jing Liu6.   

Abstract

Hematopoiesis requires finely tuned regulation of gene expression at each stage of development. The regulation of gene transcription involves not only individual transcription factors (TFs) but also transcription complexes (TCs) composed of transcription factor(s) and multisubunit cofactors. In their normal compositions, TCs orchestrate lineage-specific patterns of gene expression and ensure the production of the correct proportions of individual cell lineages during hematopoiesis. The integration of posttranslational and conformational modifications in the chromatin landscape, nucleosomes, histones and interacting components via the cofactor-TF interplay is critical to optimal TF activity. Mutations or translocations of cofactor genes are expected to alter cofactor-TF interactions, which may be causative for the pathogenesis of various hematologic disorders. Blocking TF oncogenic activity in hematologic disorders through targeting cofactors in aberrant complexes has been an exciting therapeutic strategy. In this review, we summarize the current knowledge regarding the models and functions of cofactor-TF interplay in physiological hematopoiesis and highlight their implications in the etiology of hematological malignancies. This review presents a deep insight into the physiological and pathological implications of transcription machinery in the blood system.

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Year:  2021        PMID: 33468999      PMCID: PMC7815747          DOI: 10.1038/s41392-020-00422-1

Source DB:  PubMed          Journal:  Signal Transduct Target Ther        ISSN: 2059-3635


  155 in total

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Journal:  Cell Signal       Date:  2018-11-15       Impact factor: 4.315

4.  PRDM16 Suppresses MLL1r Leukemia via Intrinsic Histone Methyltransferase Activity.

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6.  Antagonistic interactions between Ikaros and the chromatin remodeler Mi-2beta determine silencer activity and Cd4 gene expression.

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7.  Crosstalk between C/EBPbeta phosphorylation, arginine methylation, and SWI/SNF/Mediator implies an indexing transcription factor code.

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Journal:  Oncogene       Date:  2012-09-03       Impact factor: 9.867

9.  Somatic MED12 mutations are associated with poor prognosis markers in chronic lymphocytic leukemia.

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10.  GFI1 proteins orchestrate the emergence of haematopoietic stem cells through recruitment of LSD1.

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Journal:  Nat Cell Biol       Date:  2015-11-30       Impact factor: 28.824

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Review 3.  The emerging role of ISWI chromatin remodeling complexes in cancer.

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4.  Integrating transcription-factor abundance with chromatin accessibility in human erythroid lineage commitment.

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Review 5.  The transrepression and transactivation roles of CtBPs in the pathogenesis of different diseases.

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