XBP1

Information XBP1

Description

Functions as a transcription factor during endoplasmic reticulum stress by regulating the unfolded protein response (UPR). Required for cardiac myogenesis and hepatogenesis during embryonic development and the development of secretory tissues such as exocrine pancreas and salivary gland (PubMed:10425189, PubMed:10652269, PubMed:16362047, PubMed:17612490). Involved in differentiation of B lymphocytes to plasma cells and production of immunoglobulins. Modulates the cellular response to ER stress in a PIK3R-dependent manner. Binds to the cis-acting X box present in the promoter regions of major histocompatibility complex class II genes (By similarity). Involved in VEGF-induced endothelial cell (EC) proliferation and retinal blood vessel formation during embryonic development but also for angiogenesis in adult tissues under ischemic conditions (PubMed:23529610). Functions also as a major regulator of the UPR in obesity-induced insulin resistance and type 2 diabetes for the management of obesity and diabetes prevention (PubMed:15486293). {ECO:0000250|UniProtKB:P17861, ECO:0000269|PubMed:10425189, ECO:0000269|PubMed:10652269, ECO:0000269|PubMed:15486293, ECO:0000269|PubMed:16362047, ECO:0000269|PubMed:17612490, ECO:0000269|PubMed:23529610}.; [Isoform 1]: Plays a role in the unconventional cytoplasmic splicing processing of its own mRNA triggered by the endoplasmic reticulum (ER) transmembrane endoribonuclease ENR1: upon ER stress, the emerging XBP1 polypeptide chain, as part of a mRNA-ribosome-nascent chain (R-RNC) complex, cotranslationally recruits its own unprocessed mRNA through transient docking to the ER membrane and translational pausing, therefore facilitating efficient IRE1-mediated XBP1 mRNA isoform 2 production. In endothelial cells (EC), associated with KDR, promotes IRE1-mediated XBP1 mRNA isoform 2 production in a vascular endothelial growth factor (VEGF)-dependent manner, leading to EC proliferation and angiogenesis (By similarity). Functions as a negative feed-back regulator of the potent transcription factor XBP1 isoform 2 protein levels through proteasome-mediated degradation, thus preventing the constitutive activation of the ER stress response signaling pathway (PubMed:16332684). Inhibits the transactivation activity of XBP1 isoform 2 in myeloma cells (PubMed:12902539). Acts as a weak transcriptional factor. Together with HDAC3, contributes to the activation of NFE2L2-mediated HMOX1 transcription factor gene expression in a PI(3)K/mTORC2/Akt-dependent signaling pathway leading to EC survival under disturbed flow/oxidative stress. Binds to the ER stress response element (ERSE) upon ER stress. Binds to the consensus 5'-GATGACGTG[TG]N(3)[AT]T-3' sequence related to cAMP responsive element (CRE)-like sequences. Binds the Tax-responsive element (TRE) present in the long terminal repeat (LTR) of T-cell leukemia virus type 1 (HTLV-I) and to the TPA response elements (TRE). Associates preferentially to the HDAC3 gene promoter region in a static flow-dependent manner. Binds to the CDH5/VE-cadherin gene promoter region (By similarity). {ECO:0000250|UniProtKB:P17861, ECO:0000269|PubMed:12902539, ECO:0000269|PubMed:16332684}.; [Isoform 2]: Functions as a stress-inducible potent transcriptional activator during endoplasmic reticulum (ER) stress by inducing unfolded protein response (UPR) target genes via binding to the UPR element (UPRE). Up-regulates target genes encoding ER chaperones and ER-associated degradation (ERAD) components to enhance the capacity of productive folding and degradation mechanism, respectively, in order to maintain the homeostasis of the ER under ER stress (PubMed:11850408, PubMed:14559994). Plays a role in the production of immunoglobulins and interleukin-6 in the presence of stimuli required for plasma cell differentiation, and promotes as well membrane phospholipid biosynthesis necessary for ER expansion (PubMed:12612580, PubMed:17213183). Contributes to the VEGF-induced endothelial cell (EC) growth and proliferation in a Akt/GSK-dependent and/or -independent signaling pathway, respectively, leading to beta-catenin nuclear translocation and E2F2 gene expression. Promotes umbilical vein EC apoptosis and atherosclerotisis development in a caspase-dependent signaling pathway, and contributes to VEGF-induced EC proliferation and angiogenesis in adult tissues under ischemic conditions. Involved in the regulation of endostatin-induced autophagy in EC through BECN1 transcriptional activation. Plays a role as an oncogene by promoting tumor progression: stimulates zinc finger protein SNAI1 transcription to induce epithelial-to-mesenchymal (EMT) transition, cell migration and invasion of breast cancer cells (By similarity). Involved in adipocyte differentiation by regulating lipogenic gene expression during lactation (PubMed:23623498, PubMed:25223794). Plays a role in the survival of both dopaminergic neurons of the substantia nigra pars compacta (SNpc), by maintaining protein homeostasis and of myeloma cells (PubMed:12902539, PubMed:24753614). Increases insulin sensitivity in the liver as a response to a high carbohydrate diet, resulting in improved glucose tolerance (PubMed:20348926). Improves also glucose homeostasis in an ER stress- and/or insulin-independent manner through both binding and proteasome-induced degradation of the transcription factor FOXO1, hence resulting in suppression of gluconeogenic genes expression and in a reduction of blood glucose levels (PubMed:21317886). Controls the induction of de novo fatty acid synthesis in hepatocytes by regulating the expression of a subset of lipogenic genes in an ER stress- and UPR-independent manner (PubMed:18556558). Binds to the 5'-CCACG-3' motif in the PPARG promoter (PubMed:25223794). Associates preferentially to the HDAC3 gene promoter region in a disturbed flow-dependent manner. Binds to the BECN1 gene promoter region. Binds to the CDH5/VE-cadherin gene promoter region. Binds to the ER stress response element (ERSE) upon ER stress (By similarity). {ECO:0000250|UniProtKB:P17861, ECO:0000269|PubMed:11850408, ECO:0000269|PubMed:12612580, ECO:0000269|PubMed:12902539, ECO:0000269|PubMed:14559994, ECO:0000269|PubMed:17213183, ECO:0000269|PubMed:18556558, ECO:0000269|PubMed:20348926, ECO:0000269|PubMed:21317886, ECO:0000269|PubMed:23623498, ECO:0000269|PubMed:24753614, ECO:0000269|PubMed:25223794}.(Source UnitProtKB).

Full Name

X-box binding protein 1

Source UniprotKB

Species

Mus musculus [tax_id: 10090]

Genome

mm10

ReMap Statistics

Datasets
17
Biotypes
2
Peaks
297,121
Non-redundant peaks
139,368

TF Classification

Familly
NA
Sub Familly
NA

Source JASPAR

External IDs

NCBI Gene
22433
Official Gene Name
Xbp1
JASPAR
MGI
MGI:98970
Ensembl
ENSMUSG00000020484
UniProt
O35426
Genevisible
O35426
RefSeq
NM_013842
Aliases
D11Ertd39e; TREB-5; TREB5; XBP-1
All peaks XBP1
Download BED file
Non redundant peaks XBP1
Download BED file
SEQUENCES XBP1
Download FASTA file
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Datasets Table for XBP1

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
XBP1 liver fasted GEO Mus musculus GSE101202 40,400
XBP1 liver PH-48h GEO Mus musculus GSE86048 28,132
XBP1 liver SHAM-6h GEO Mus musculus GSE86048 51,380
XBP1 liver GEO Mus musculus GSE86048 7,690
XBP1 liver CT20 GEO Mus musculus GSE130760 122
XBP1 liver GEO Mus musculus GSE101202 22,367
XBP1 liver PH-6h_shXbp1 GEO Mus musculus GSE86048 13,604
XBP1 liver T12 GEO Mus musculus GSE130760 222
XBP1 liver SHAM-48h GEO Mus musculus GSE86048 8,682
XBP1 liver T36 GEO Mus musculus GSE130760 328
XBP1 liver PH-6h GEO Mus musculus GSE86048 32,712
XBP1 liver CT36 GEO Mus musculus GSE130760 328
XBP1 liver CT12 GEO Mus musculus GSE130760 222
XBP1 liver Ern1-LKO GEO Mus musculus GSE101202 15,785
XBP1 liver fed GEO Mus musculus GSE101202 74,720
XBP1 liver T20 GEO Mus musculus GSE130760 122
XBP1 AtT-20 GEO Mus musculus GSE132320 305
Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks