This gene encodes a transcription factor that regulates MHC class II genes by binding to a promoter element referred to as an X box. This gene product is a bZIP protein, which was also identified as a cellular transcription factor that binds to an enhancer in the promoter of the T cell leukemia virus type 1 promoter. It may increase expression of viral proteins by acting as the DNA binding partner of a viral transactivator. It has been found that upon accumulation of unfolded proteins in the endoplasmic reticulum (ER), the mRNA of this gene is processed to an active form by an unconventional splicing mechanism that is mediated by the endonuclease inositol-requiring enzyme 1 (IRE1). The resulting loss of 26 nt from the spliced mRNA causes a frame-shift and an isoform XBP1(S), which is the functionally active transcription factor. The isoform encoded by the unspliced mRNA, XBP1(U), is constitutively expressed, and thought to function as a negative feedback regulator of XBP1(S), which shuts off transcription of target genes during the recovery phase of ER stress. A pseudogene of XBP1 has been identified and localized to chromosome 5. [provided by RefSeq, Jul 2008]
Transcription factors with Perturb-seq knockdown data for XBP1. The Binding column indicates whether any binding evidence exists for this TF–gene pair (ChIP-seq or motif footprint peaks). The Mean coef is the average Perturb-seq regression coefficient across active gRNAs (positive = XBP1 upregulated upon KD; negative = downregulated). The Outlier column indicates whether this gene is in the top or bottom 5% of all TF knockdown effects.
| TF | Mean coef | Binding | Outlier | TF→Gene link |
|---|
Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of XBP1, linked by TSS proximity or chromatin conformation (Multiome / HiCAR). Each element overlaps at least one TF ChIP-seq binding site — the TFs column shows how many distinct TFs bind that element.
| Accessibility | Element | Dist. to TSS | Link type | TFs |
|---|---|---|---|---|
| chr22:28,679,491–28,680,261 | 120.7 kb | Distal (>10kb) Multiome | 374 | |
| chr22:28,741,336–28,742,751 | 58.7 kb | Distal (>10kb) Multiome | 926 | |
| chr22:28,772,518–28,773,373 | 27.8 kb | Distal (>10kb) Multiome | 796 | |
| chr22:28,800,006–28,801,035 | 31 bp | At TSS Multiome | 829 | |
| chr22:28,882,670–28,884,893 | 82.8 kb | Distal (>10kb) Multiome | 802 | |
| chr22:29,004,535–29,005,249 | 204.4 kb | Distal (>10kb) Multiome | 417 | |
| chr22:29,029,712–29,031,115 | 230.3 kb | Distal (>10kb) Multiome | 773 | |
| chr22:29,071,484–29,071,874 | 271.0 kb | Distal (>10kb) Multiome | 332 | |
| chr22:29,072,494–29,074,480 | 272.4 kb | Distal (>10kb) Multiome | 537 |
Genomic view of the XBP1 locus showing ATAC-seq accessibility and RNA-seq expression across the ESC → DE time course, together with TF binding peaks and element-to-TSS loop connections.