Edge Rewrite
// HTMLRewriter · presentation

This page was redesigned at the edge.

Cloudflare fetched the original article and streamed it through HTMLRewriter to apply an entirely new visual system without rebuilding the source page.

// request.cf · coarse context

A page that knows where it met you.

Only coarse request metadata is shown. This demo does not display or persist visitor IP addresses.

Country
US
Cloudflare location
CMH
Connection
HTTP/2
Language
Not provided

Ray ID: a22b85294900a9c0

Jump to content

CoREST

From Wikipedia, the free encyclopedia

CoREST is a family of closely related corepressor proteins. These proteins down regulate gene expression, not by directly binding to DNA, but rather by binding to and enhancing the activity repressor proteins. In humans, there are three CoREST paralogs: RCOR1 (CoREST1), RCOR2 (CoREST2), and RCOR3 (CoREST3).[1]

CoREST proteins directly interact with RE1-silencing transcription factor (REST).[2] The REST/CoREST complex includes REST, one CoREST paralog (RCOR1, RCOR2, or RCOR3), LSD1/KDM1A, and HDAC1 or HDAC2.[3]

The REST/CoREST/LSD1/HDAC complex couples transcriptional repression (REST) to histone demethylation (LSD1) and deacetylation (HDAC1/2).[4]

CoREST proteins contain an N-terminal ELM2 domain followed by a central SANT domain pair and a C-terminal region that mediates protein interactions. The first SANT domain (SANT1), together with ELM2, are involved in HDAC1/2 recruitment, while the second SANT domain (SANT2) together with the linker regions between SANT1 and SANT2 binds to LSD1/KDM1A.[4] The C-terminal region of CoREST1 and CoREST3 contain several coiled-coil regions that may mediate additional protein-protein interactions.[4]

References

[edit]
  1. Barrios ÁP, Gómez AV, Sáez JE, Ciossani G, Toffolo E, Battaglioli E, Mattevi A, Andrés ME (July 2014). "Differential properties of transcriptional complexes formed by the CoREST family". Molecular and Cellular Biology. 34 (14): 2760–70. doi:10.1128/MCB.00083-14. PMC 4097654. PMID 24820421.
  2. Qureshi IA, Gokhan S, Mehler MF (November 2010). "REST and CoREST are transcriptional and epigenetic regulators of seminal neural fate decisions". Cell Cycle. 9 (22). Georgetown, Tex.: 4477–86. doi:10.4161/cc.9.22.13973. PMC 3048046. PMID 21088488.
  3. Ismail H, Chagraoui J, Sauvageau G (June 2025). "CoREST in pieces: Dismantling the CoREST complex for cancer therapy and beyond". Science Advances. 11 (23) eads6556. doi:10.1126/sciadv.ads6556. PMC 12143397. PMID 40479062.
  4. 1 2 3 Maksour S, Ooi L, Dottori M (2020). "More than a Corepressor: The Role of CoREST Proteins in Neurodevelopment". eNeuro. 7 (2). doi:10.1523/ENEURO.0337-19.2020. PMC 7070449. PMID 32075869.