Literature DB >> 28960081

Systematic Proteogenomic Approach To Exploring a Novel Function for NHERF1 in Human Reproductive Disorder: Lessons for Exploring Missing Proteins.

Keun Na1, Heon Shin2, Jin-Young Cho1, Sang Hee Jung3, Jaeseung Lim4, Jong-Sun Lim1, Eun Ah Kim3, Hye Sun Kim4, Ah Reum Kang4, Ji Hye Kim4, Jeong Min Shin5, Seul-Ki Jeong1, Chae-Yeon Kim2, Jun Young Park2, Hyung-Min Chung6, Gilbert S Omenn7, William S Hancock8, Young-Ki Paik1,2,9.   

Abstract

One of the major goals of the Chromosome-Centric Human Proteome Project (C-HPP) is to fill the knowledge gaps between human genomic information and the corresponding proteomic information. These gaps are due to "missing" proteins (MPs)-predicted proteins with insufficient evidence from mass spectrometry (MS), biochemical, structural, or antibody analyses-that currently account for 2579 of the 19587 predicted human proteins (neXtProt, 2017-01). We address some of the lessons learned from the inconsistent annotations of missing proteins in databases (DB) and demonstrate a systematic proteogenomic approach designed to explore a potential new function of a known protein. To illustrate a cautious and strategic approach for characterization of novel function in vitro and in vivo, we present the case of Na(+)/H(+) exchange regulatory cofactor 1 (NHERF1/SLC9A3R1, located at chromosome 17q25.1; hereafter NHERF1), which was mistakenly labeled as an MP in one DB (Global Proteome Machine Database; GPMDB, 2011-09 release) but was well known in another public DB and in the literature. As a first step, NHERF1 was determined by MS and immunoblotting for its molecular identity. We next investigated the potential new function of NHERF1 by carrying out the quantitative MS profiling of placental trophoblasts (PXD004723) and functional study of cytotrophoblast JEG-3 cells. We found that NHERF1 was associated with trophoblast differentiation and motility. To validate this newly found cellular function of NHERF1, we used the Caenorhabditis elegans mutant of nrfl-1 (a nematode ortholog of NHERF1), which exhibits a protruding vulva (Pvl) and egg-laying-defective phenotype, and performed genetic complementation work. The nrfl-1 mutant was almost fully rescued by the transfection of the recombinant transgenic construct that contained human NHERF1. These results suggest that NHERF1 could have a previously unknown function in pregnancy and in the development of human embryos. Our study outlines a stepwise experimental platform to explore new functions of ambiguously denoted candidate proteins and scrutinizes the mandated DB search for the selection of MPs to study in the future.

Entities:  

Keywords:  C-HPP; NHERF1; SLC9A3R1; missing protein; preeclampsia; proteogenomics

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Year:  2017        PMID: 28960081      PMCID: PMC6610236          DOI: 10.1021/acs.jproteome.7b00146

Source DB:  PubMed          Journal:  J Proteome Res        ISSN: 1535-3893            Impact factor:   4.466


  3 in total

Review 1.  Progress on Identifying and Characterizing the Human Proteome: 2018 Metrics from the HUPO Human Proteome Project.

Authors:  Gilbert S Omenn; Lydie Lane; Christopher M Overall; Fernando J Corrales; Jochen M Schwenk; Young-Ki Paik; Jennifer E Van Eyk; Siqi Liu; Michael Snyder; Mark S Baker; Eric W Deutsch
Journal:  J Proteome Res       Date:  2018-08-23       Impact factor: 4.466

Review 2.  Advances in the Chromosome-Centric Human Proteome Project: looking to the future.

Authors:  Young-Ki Paik; Gilbert S Omenn; William S Hancock; Lydie Lane; Christopher M Overall
Journal:  Expert Rev Proteomics       Date:  2017-11-10       Impact factor: 3.940

3.  ERM-1 Phosphorylation and NRFL-1 Redundantly Control Lumen Formation in the C. elegans Intestine.

Authors:  Jorian J Sepers; João J Ramalho; Jason R Kroll; Ruben Schmidt; Mike Boxem
Journal:  Front Cell Dev Biol       Date:  2022-02-07
  3 in total

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