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GeneQ18035105· pop 5· linked from 6 articles

Also known as ALY, ALY/REF, BEF, REF, THOC4, Aly/REF export factor

Aly/REF export factor, also known as THO complex subunit 4 is a protein that in humans is encoded by the ALYREF gene.

In the Vinony graph

Within Vinony's link graph, ALYREF is referenced by 6 other articles, and connects out to PubMed, human chromosome 17 and Ensembl genome database project.

It is catalogued under the topic Genes on human chromosome 17.

Its subject is documented across 4 Wikipedia language editions.

Gene data

ALYREF
Name
Aly/REF export factor
Type
protein-coding
Position
81,887,830–81,891,835 (−)
Aliases
ALY, ALY/REF, BEF, REF, THOC4
RefSeq RNA
NM_005782.4, NR_158770.1
RefSeq protein
NP_005773.3

The protein encoded by this gene is a heat stable, nuclear protein and functions as a molecular chaperone. It is thought to regulate dimerization, DNA binding, and transcriptional activity of basic region-leucine zipper (bZIP) proteins. [provided by RefSeq, Jul 2008].

via MyGene.info

Gene · Ensembl

Aly/REF export factor

Symbol
ALYREF
Biotype
Protein coding
Organism
Homo sapiens
Location
17:81,887,830-81,891,835
Strand
Reverse (−)
Assembly
GRCh38
View on Ensembl →

via Ensembl · EMBL-EBI

Wikidata facts

Instance of
gene
Image
Protein THOC4 PDB 1no8.png
Show 7 more facts
HomoloGene ID
134554
found in taxon
Homo sapiens
genomic end
79849462
genomic start
81887835
cytogenetic location
17q25.3
Sources (4)

via Wikidata · CC0

~2 min read

Encyclopedic overview

3 sections
Contents
  • References
  • Further reading
  • External links

Aly/REF export factor, also known as THO complex subunit 4 is a protein that in humans is encoded by the ALYREF gene.

The ALYREF gene encodes Aly/REF export factor (ALY; THO complex subunit 4, Tho4; RNA and export factor binding protein 1, Refbp1), a ubiquitously expressed nuclear protein that functions as a molecular chaperone and export adapter involved in nuclear export of spliced and unspliced mRNA. The TRanscription-EXport (TREX) complex, a key player in mRNA export, includes the THO subcomplex, the RNA helicase UAP56, and the RNA-binding protein ALY. In yeast, TREX is recruited co-transcriptionally; in human cells it is recruited during a late step of splicing. The human TREX complex is recruited to a region near the 5' end of mRNA by interaction of ALY and THO with the nuclear cap-binding complex. As a chaperone, ALY promotes dimerization of transcription factors containing basic leucine zipper (bZIP) domains., thereby promoting transcriptional activation. ALY has key roles in 3'-end processing of polyadenylated mRNAs and in nuclear export of both polyadenylated and non-polyadenylated mRNAs. After mRNA binds to ALY, it is apparently transferred to the NXF1-NXT1 heterodimer for export (TAP/NFX1 pathway). The full-length ALY protein (Refbp1-I, 255 amino acids encoded by six exons) has a conserved RNA recognition motif (RRM; amino acids 105-182) flanked by alanine/arginine/glycine-rich sequences; an N-terminal region (amino acids 16-37) is sufficient for RNA binding and interaction with the NXF1-NXT1 heterodimer.

Excerpted from Wikipedia’s “ALYREF” article, available under the CC BY-SA 4.0 licence.

Available in 4 languages

via Wikidata sitelinks · CC0

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