EBF1

From WikiMD's medical encyclopedia

Gene
Symbol
HGNC ID
Alternative symbols
Entrez Gene
OMIM
RefSeq
UniProt
Chromosome
Locus supplementary data

EBF1 (Early B-cell Factor 1) is a protein that in humans is encoded by the EBF1 gene. This protein is a member of the Olf/EBF family of transcription factors which play a critical role in B cell development.

Function

EBF1 is a helix-loop-helix transcription factor that is important for the differentiation of early B cell progenitors. It is not only essential in lymphocyte development but also participates in the regulation of gene expression during the maturation of B cells. EBF1 binds to a specific DNA sequence and acts as a transcriptional activator or repressor, depending on the context of the cell's environment and developmental stage.

Clinical Significance

Alterations in the expression of EBF1 have been associated with various hematological disorders and cancers, particularly those affecting the B cells such as acute lymphoblastic leukemia (ALL). Studies suggest that EBF1 plays a role in the pathogenesis of these diseases by influencing cell cycle progression and apoptosis in B cells.

Genetic Structure

The EBF1 gene is located on chromosome 5 (5q33.3) in humans. It consists of multiple exons that span a significant portion of the chromosome. The gene encodes a protein that is involved in numerous cellular processes, including cell differentiation and response to external signals.

Research

Research on EBF1 continues to uncover its roles not only in normal B cell development but also in the development of B cell malignancies. Understanding the mechanisms by which EBF1 regulates these processes is crucial for developing targeted therapies for related diseases.

See Also

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Contributors: Prab R. Tumpati, MD