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Shared transcription factors contribute to distinct cell fates.


Type

Article

Change log

Authors

Ng, Felicia SL 
Calero-Nieto, Fernando J 
Göttgens, Berthold 

Abstract

Genome-wide transcription factor (TF) binding profiles differ dramatically between cell types. However, not much is known about the relationship between cell-type-specific binding patterns and gene expression. A recent study demonstrated how the same TFs can have functional roles when binding to largely non-overlapping genomic regions in hematopoietic progenitor and mast cells. Cell-type specific binding profiles of shared TFs are therefore not merely the consequence of opportunistic and functionally irrelevant binding to accessible chromatin, but instead have the potential to make meaningful contributions to cell-type specific transcriptional programs.

Description

Keywords

ChIP-seq, ChIP sequencing, GAM, generalized additive model, RNA-seq, RNA sequencing, TF, transcription factor, binding motif, hematopoiesis, mast cell, regression model, Animals, Cell Lineage, Gene Expression, Humans, Organ Specificity, Transcription Factors

Journal Title

Transcription

Conference Name

Journal ISSN

2154-1264
2154-1272

Volume Title

5

Publisher

Informa UK Limited

Rights

Attribution 2.0 UK: England & Wales
Sponsorship
Cancer Research Uk (None)
Biotechnology and Biological Sciences Research Council (BB/I00050X/1)
Leukaemia & Lymphoma Research (12029)
Wellcome Trust (097922/Z/11/Z)
Medical Research Council (MC_PC_12009)
Leukemia & Lymphoma Society (7001-12)
Work in the authors’ laboratory is supported by grants from Leukaemia and Lymphoma Research, the MRC, BBSRC, the Leukaemia and Lymphoma Society, Cancer Research UK, the National Institute for Health Research Cambridge Biomedical Research Centre, and core support grants by the Wellcome Trust to the Cambridge Institute for Medical Research and Wellcome Trust & MRC Cambridge Stem Cell Institute. FSLN is the recipient of a Yousef Jameel scholarship.