Proteomics

Dataset Information

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Protein interactome profiling of ER alpha by RIME assay from the human hepatocellular cancer HepG2 stable cells


ABSTRACT: Estrogeh insensitivity syndrome (EIS) arises from rare mutations in ERα resulting in the inability of estrogen to exert its biological effects. Due to the rarity, mutations in ESR1 gene and the underlying molecular mechanisms of EIS have not been thoroughly studied. We used RIME (Rapid Immunoprecipitation Mass spectrometry of Endogenous proteins) analysis to compare the interactions for ER alpha between the WT ER alpha and Q375H clinical mutant in HepG2 stable cells.

INSTRUMENT(S): LTQ

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Cell Culture

SUBMITTER: Yin Li  

LAB HEAD: Yin Li

PROVIDER: PXD020666 | Pride | 2021-09-09

REPOSITORIES: Pride

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Publications

A mutant form of ERα associated with estrogen insensitivity affects the coupling between ligand binding and coactivator recruitment.

Li Yin Y   Coons Laurel A LA   Houtman René R   Carlson Kathryn E KE   Martin Teresa A TA   Mayne Christopher G CG   Melchers Diana D   Jefferson Tanner B TB   Ramsey J Tyler JT   Katzenellenbogen John A JA   Korach Kenneth S KS  

Science signaling 20200922 650


A homozygous missense mutation in the gene encoding the estrogen receptor α (ERα) was previously identified in a female patient with estrogen insensitivity syndrome. We investigated the molecular features underlying the impaired transcriptional response of this mutant (ERα-Q375H) and four other missense mutations at this position designed to query alternative mechanisms. The identity of residue 375 greatly affected the sensitivity of the receptor to agonists without changing the ligand binding a  ...[more]

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