XBP1

Source: Wikipedia, the free encyclopedia.
XBP1
Identifiers
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Ensembl
UniProt
RefSeq (mRNA)

NM_005080
NM_001079539
NM_001393999
NM_001394000

NM_001271730
NM_013842

RefSeq (protein)

NP_001073007
NP_005071

NP_001258659
NP_038870

Location (UCSC)Chr 22: 28.79 – 28.8 MbChr 11: 5.47 – 5.48 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

X-box binding protein 1, also known as XBP1, is a protein which in humans is encoded by the XBP1 gene.[5][6] The XBP1 gene is located on chromosome 22 while a closely related pseudogene has been identified and localized to chromosome 5.[7] The XBP1 protein is a transcription factor that regulates the expression of genes important to the proper functioning of the immune system and in the cellular stress response.[8]

Discovery

The X-box binding protein 1 (XBP1) is a

promoter of the human leukocyte antigen (HLA) DR alpha.[6]

Function

MHC class II gene regulation

The expression of this protein is required for the transcription of a subset of

XBP1 expression is controlled by the

Plasma cell differentiation

XBP1 is also essential for differentiation of plasma cells (a type of antibody secreting immune cell).[10] This differentiation requires not only the expression of XBP1 but the expression of the spliced isoform of XBP1s. XBP1 regulates plasma cell differentiation independent of its known functions in the endoplasmic reticulum stress response (see below).[11] Without normal expression of XBP1, two important plasma cell differentiation-related genes, IRF4 and Blimp1, are misregulated, and XBP1-lacking plasma cells fail to colonize their long-lived niches in the bone marrow and to sustain antibody secretion.[11]

Eosinophil differentiation

XBP1 is required for eosinophil differentiation. Eosinophils lacking XBP1 exhibit defects in granule proteins.[12]

Angiogenesis

XBP1 acts to regulate endothelial cell proliferation through growth factor pathways,[13] leading to angiogenesis. Additionally, XBP1 protects endothelial cells from oxidative stress by interacting with HDAC3.[14]

Viral replication

This protein has also been identified as a cellular transcription factor that binds to an enhancer in the promoter of the

Epstein Barr virus
reactivation from latency.

Endoplasmic reticulum stress response

XBP1 is part of the

isoform
rather than the 261 amino acid, 33 kDa, XBP1u isoform. Moreover, the XBP1u/XBP1s ratio (XBP1-unspliced/XBP1-spliced ratio) correlates with the expression level of expressed proteins in order to adapt the folding capacity of the ER to the respective requirements.[17]

Clinical significance

Abnormalities in XBP1 lead to a heightened ER stress and subsequently causes a heightened susceptibility for inflammatory processes that may contribute to

colon, XBP1 anomalies have been linked to Crohn's disease.[19]

A

personality traits. None were found.[20]

Interactions

XBP1 has been shown to

See also

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000100219Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000020484Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: XBP1 X-box binding protein 1".
  6. ^
    PMID 2321018
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