Liu, Yansheng ORCID: 0000-0002-2626-3912, Borel, Christelle, Li, Li, Mueller, Torsten, Williams, Evan G., Germain, Pierre-Luc, Buljan, Marija, Sajic, Tatjana, Boersema, Paul J., Shao, Wenguang, Faini, Marco, Testa, Giuseppe ORCID: 0000-0002-9104-0918, Beyer, Andreas ORCID: 0000-0002-3891-2123, Antonarakis, Stylianos E. and Aebersold, Ruedi ORCID: 0000-0002-9576-3267 (2017). Systematic proteome and proteostasis profiling in human Trisomy 21 fibroblast cells. Nat. Commun., 8. LONDON: NATURE PUBLISHING GROUP. ISSN 2041-1723

Full text not available from this repository.

Abstract

Down syndrome (DS) is mostly caused by a trisomy of the entire Chromosome 21 (Trisomy 21, T21). Here, we use SWATH mass spectrometry to quantify protein abundance and protein turnover in fibroblasts from a monozygotic twin pair discordant for T21, and to profile protein expression in 11 unrelated DS individuals and matched controls. The integration of the steady-state and turnover proteomic data indicates that protein-specific degradation of members of stoichiometric complexes is a major determinant of T21 gene dosage outcome, both within and between individuals. This effect is not apparent from genomic and transcriptomic data. The data also reveal that T21 results in extensive proteome remodeling, affecting proteins encoded by all chromosomes. Finally, we find broad, organelle-specific post-transcriptional effects such as significant downregulation of the mitochondrial proteome contributing to T21 hallmarks. Overall, we provide a valuable proteomic resource to understand the origin of DS phenotypic manifestations.

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Liu, YanshengUNSPECIFIEDorcid.org/0000-0002-2626-3912UNSPECIFIED
Borel, ChristelleUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Li, LiUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Mueller, TorstenUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Williams, Evan G.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Germain, Pierre-LucUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Buljan, MarijaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Sajic, TatjanaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Boersema, Paul J.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Shao, WenguangUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Faini, MarcoUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Testa, GiuseppeUNSPECIFIEDorcid.org/0000-0002-9104-0918UNSPECIFIED
Beyer, AndreasUNSPECIFIEDorcid.org/0000-0002-3891-2123UNSPECIFIED
Antonarakis, Stylianos E.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Aebersold, RuediUNSPECIFIEDorcid.org/0000-0002-9576-3267UNSPECIFIED
URN: urn:nbn:de:hbz:38-213817
DOI: 10.1038/s41467-017-01422-6
Journal or Publication Title: Nat. Commun.
Volume: 8
Date: 2017
Publisher: NATURE PUBLISHING GROUP
Place of Publication: LONDON
ISSN: 2041-1723
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
GENE-EXPRESSION VARIATION; DOWN-SYNDROME; MITOCHONDRIAL DYSFUNCTION; PEPTIDE IDENTIFICATION; QUANTIFICATION; CHROMOSOME-21; DEGRADATION; DYNAMICS; REVEALS; DOSAGEMultiple languages
Multidisciplinary SciencesMultiple languages
Refereed: Yes
URI: http://kups.ub.uni-koeln.de/id/eprint/21381

Downloads

Downloads per month over past year

Altmetric

Export

Actions (login required)

View Item View Item