Transcription factor EBF1 is essential for the maintenance of B cell identity and prevention of alternative fates in committed cells. (Q44979321)

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4 March 2020

title

Transcription factor EBF1 is essential for the maintenance of B cell identity and prevention of alternative fates in committed cells (English)

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4 March 2020

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Robert Nechanitzky

1

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4 March 2020

Duygu Akbas

2

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4 March 2020

Stefanie Scherer

3

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4 March 2020

Ildiko Györy

4

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4 March 2020

Thomas Hoyler

5

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4 March 2020

Rudolf Grosschedl

8

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4 March 2020

language of work or name

English

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publication date

30 June 2013

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4 March 2020

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23812095 AND SRC:MED&resulttype=core&format=json

4 March 2020

volume

14

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4 March 2020

issue

8

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4 March 2020

page(s)

867-875

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Conversion of mature B cells into T cells by dedifferentiation to uncommitted progenitors

4 March 2020

cites work

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12 December 2020

The transcriptional regulation of B cell lineage commitment.

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Positive intergenic feedback circuitry, involving EBF1 and FOXO1, orchestrates B-cell fate

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A global network of transcription factors, involving E2A, EBF1 and Foxo1, that orchestrates B cell fate

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Transcription factor Ebf1 regulates differentiation stage-specific signaling, proliferation, and survival of B cells

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Transcriptional drivers of the T-cell lineage program

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Ly6d marks the earliest stage of B-cell specification and identifies the branchpoint between B-cell and T-cell development

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T Cell Lineage Commitment: Identity and Renunciation

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The transcription factor Pax5 regulates its target genes by recruiting chromatin-modifying proteins in committed B cells

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Reversion of B cell commitment upon loss of Pax5 expression

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Functional diversity of stem and progenitor cells with B-lymphopoietic potential

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Notch signaling controls the generation and differentiation of early T lineage progenitors

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A robust and highly efficient immune cell reprogramming system

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GATA-3 promotes T-cell specification by repressing B-cell potential in pro-T cells in mice

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T-cell factor 1 is a gatekeeper for T-cell specification in response to Notch signaling.

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Genome-wide lineage-specific transcriptional networks underscore Ikaros-dependent lymphoid priming in hematopoietic stem cells

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Transcription from the RAG1 locus marks the earliest lymphocyte progenitors in bone marrow

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Transcription factor EBF restricts alternative lineage options and promotes B cell fate commitment independently of Pax5.

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Role of Deltex-1 as a transcriptional regulator downstream of the Notch receptor

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Single-cell analysis of early B-lymphocyte development suggests independent regulation of lineage specification and commitment in vivo.

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Testing gene function early in the B cell lineage in mb1-cre mice

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Ebf1-mediated down-regulation of Id2 and Id3 is essential for specification of the B cell lineage

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The transcription factor GATA-3 controls cell fate and maintenance of type 2 innate lymphoid cells.

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Stepwise activation of enhancer and promoter regions of the B cell commitment gene Pax5 in early lymphopoiesis

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B-lymphocyte commitment: identifying the point of no return

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Innate production of T(H)2 cytokines by adipose tissue-associated c-Kit( )Sca-1( ) lymphoid cells

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Early B cell factor promotes B lymphopoiesis with reduced interleukin 7 responsiveness in the absence of E2A

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12 December 2020

A dose-dependent role for EBF1 in repressing non-B-cell-specific genes.

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Early B cell factor 2 regulates hematopoietic stem cell homeostasis in a cell-nonautonomous manner.

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Distinct functions for the transcription factor Foxo1 at various stages of B cell differentiation

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Innate lymphoid cells--a proposal for uniform nomenclature

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Transcription control of early B cell differentiation

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12 December 2020

Early B cell factor 1 regulates B cell gene networks by activation, repression, and transcription- independent poising of chromatin

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12 December 2020

Distinct promoters mediate the regulation of Ebf1 gene expression by interleukin-7 and Pax5

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A critical role for TCF-1 in T-lineage specification and differentiation

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Regulation of B cell fate commitment and immunoglobulin heavy-chain gene rearrangements by Ikaros.

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Transcriptional control of innate lymphocyte fate decisions.

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Long-term in vivo reconstitution of T-cell development by Pax5-deficient B-cell progenitors

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Essential role of EBF1 in the generation and function of distinct mature B cell types

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12 December 2020

Commitment to the B-lymphoid lineage depends on the transcription factor Pax5

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12 December 2020

Multilineage priming of enhancer repertoires precedes commitment to the B and myeloid cell lineages in hematopoietic progenitors.

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12 December 2020

Assembling a gene regulatory network for specification of the B cell fate

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12 December 2020

Gene repression by Pax5 in B cells is essential for blood cell homeostasis and is reversed in plasma cells

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Developmental plasticity of lymphocytes

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12 December 2020