» Articles » PMID: 12505151

Characterization of a New Family of Proteins That Interact with the C-terminal Region of the Chromatin-remodeling Factor CHD-3

Overview
Journal FEBS Lett
Specialty Biochemistry
Date 2002 Dec 31
PMID 12505151
Citations 26
Authors
Affiliations
Soon will be listed here.
Abstract

The two human proteins Ki-1/57 and CGI-55 have highly similar amino acid sequences but their functions are unknown. We analyzed them by yeast two-hybrid screens and found that they interact with the C-terminal region of the human chromatin-remodeling factor CHD-3 (chromo-helicase-DNA-binding domain protein-3). The interaction of CGI-55 and CHD-3 could be confirmed in vitro and in vivo by co-immunoprecipitations from Sf9 insect cells. Mapping showed that CGI-55 interacts with CHD-3 via two regions at its N- and C-terminals. The CGI-55 and Ki-1/57 mRNAs show highest expression in muscle, colon and kidney. A CGI55-GFP fusion protein was localized in the cytoplasm, nucleus and perinuclear regions of HeLa cells. These data suggest the possibility that CGI-55 and Ki-1/57 might be involved in nuclear functions like the remodeling of chromatin.

Citing Articles

Vacuolar ATPase Is a Possible Therapeutic Target in Acute Myeloid Leukemia: Focus on Patient Heterogeneity and Treatment Toxicity.

Bartaula-Brevik S, Leitch C, Hernandez-Valladares M, Aasebo E, Berven F, Selheim F J Clin Med. 2023; 12(17).

PMID: 37685612 PMC: 10488188. DOI: 10.3390/jcm12175546.


Latency-associated upregulation of SERBP1 is important for the recruitment of transcriptional repressors to the viral major immediate early promoter of human cytomegalovirus during latent carriage.

Poole E, Sinclair J Front Microbiol. 2022; 13:999290.

PMID: 36504797 PMC: 9729347. DOI: 10.3389/fmicb.2022.999290.


NuRD complex recruitment to Thpok mediates CD4 T cell lineage differentiation.

Gao Y, Zamisch M, Vacchio M, Chopp L, Ciucci T, Paine E Sci Immunol. 2022; 7(72):eabn5917.

PMID: 35687698 PMC: 9484726. DOI: 10.1126/sciimmunol.abn5917.


Silencing of Ago-2 Interacting Protein SERBP1 Relieves KCC2 Repression by miR-92 in Neurons.

Barbato C, Frisone P, Braccini L, DAguanno S, Pieroni L, Ciotti M Cells. 2022; 11(6).

PMID: 35326503 PMC: 8947033. DOI: 10.3390/cells11061052.


A genetically-encoded crosslinker screen identifies SERBP1 as a PKCε substrate influencing translation and cell division.

Martini S, Davis K, Faraway R, Elze L, Lockwood N, Jones A Nat Commun. 2021; 12(1):6934.

PMID: 34836941 PMC: 8626422. DOI: 10.1038/s41467-021-27189-5.