» Articles » PMID: 15742316

Large-scale Identification of Proteins Expressed in Mouse Embryonic Stem Cells

Overview
Journal Proteomics
Date 2005 Mar 3
PMID 15742316
Citations 31
Authors
Affiliations
Soon will be listed here.
Abstract

A protein subset expressed in the mouse embryonic stem (ES) cell line, E14-1, was characterized by mass spectrometry-based protein identification technology and data analysis. In total, 1790 proteins including 365 potential nuclear and 260 membrane proteins were identified from tryptic digests of total cell lysates. The subset contained a variety of proteins in terms of physicochemical characteristics, subcellular localization, and biological function as defined by Gene Ontology annotation groups. In addition to many housekeeping proteins found in common with other cell types, the subset contained a group of regulatory proteins that may determine unique ES cell functions. We identified 39 transcription factors including Oct-3/4, Sox-2, and undifferentiated embryonic cell transcription factor I, which are characteristic of ES cells, 88 plasma membrane proteins including cell surface markers such as CD9 and CD81, 44 potential proteinaceous ligands for cell surface receptors including growth factors, cytokines, and hormones, and 100 cell signaling molecules. The subset also contained the products of 60 ES-specific and 41 stemness genes defined previously by the DNA microarray analysis of Ramalho-Santos et al. (Ramalho-Santos et al., Science 2002, 298, 597-600), as well as a number of components characteristic of differentiated cell types such as hematopoietic and neural cells. We also identified potential post-translational modifications in a number of ES cell proteins including five Lys acetylation sites and a single phosphorylation site. To our knowledge, this study provides the largest proteomic dataset characterized to date for a single mammalian cell species, and serves as a basic catalogue of a major proteomic subset that is expressed in mouse ES cells.

Citing Articles

Safety assessment of rat embryonic fraction for in vivo regenerative therapy.

Darsi S, Baishya S, Nagati V, Bharani K, Cheekatla S, Darsi S Biol Open. 2024; 13(8).

PMID: 38984587 PMC: 11360137. DOI: 10.1242/bio.060266.


Pluripotency state regulates cytoneme selectivity and self-organization of embryonic stem cells.

Junyent S, Reeves J, Gentleman E, Habib S J Cell Biol. 2021; 220(4).

PMID: 33606876 PMC: 7903188. DOI: 10.1083/jcb.202005095.


Specialized cytonemes induce self-organization of stem cells.

Junyent S, Garcin C, Szczerkowski J, Trieu T, Reeves J, Habib S Proc Natl Acad Sci U S A. 2020; 117(13):7236-7244.

PMID: 32184326 PMC: 7132109. DOI: 10.1073/pnas.1920837117.


Multi-omic Profiling Reveals Dynamics of the Phased Progression of Pluripotency.

Yang P, Humphrey S, Cinghu S, Pathania R, Oldfield A, Kumar D Cell Syst. 2019; 8(5):427-445.e10.

PMID: 31078527 PMC: 6544180. DOI: 10.1016/j.cels.2019.03.012.


Human CYP2A13 and CYP2F1 Mediate Naphthalene Toxicity in the Lung and Nasal Mucosa of CYP2A13/2F1-Humanized Mice.

Li L, Carratt S, Hartog M, Kovalchik N, Jia K, Wang Y Environ Health Perspect. 2017; 125(6):067004.

PMID: 28599267 PMC: 5743450. DOI: 10.1289/EHP844.