Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary for 2.3.1.6 extracted from

  • Winick-Ng, W.; Caetano, F.A.; Winick-Ng, J.; Morey, T.M.; Heit, B.; Rylett, R.J.
    82-kDa choline acetyltransferase and SATB1 localize to beta-amyloid induced matrix attachment regions (2016), Sci. Rep., 6, 23914 .
    View publication on PubMedView publication on EuropePMC

Localization

Localization Comment Organism GeneOntology No. Textmining
nucleus nuclei of cholinergic neurons Homo sapiens 5634
-

Organism

Organism UniProt Comment Textmining
Homo sapiens P28329
-
-

Source Tissue

Source Tissue Comment Organism Textmining
neuron
-
Homo sapiens
-

Subunits

Subunits Comment Organism
? x * 82000, calculated from sequence Homo sapiens

General Information

General Information Comment Organism
physiological function acute exposure to amyloid Abeta1-42 results in increased association of ChAT with chromatin and formation of ChAT aggregates in nuclei. Abeta1-42 -exposure increases ChAT association with gene promoters and introns. The Abeta1-42 -induced ChAT aggregates colocalize with special AT-rich binding protein 1 (SATB1), which anchors DNA to scaffolding/matrix attachment regions (S/MARs). Both ChAT and SATB proteins associate with synapse and cell stress genes. After Abeta1-42 -exposure, both SATB1 and ChAT are enriched at the same S/MAR on the APP gene, with ChAT expression attenuating an increase in an isoform-specific APP mRNA transcript Homo sapiens