Variable Glutamine-Rich Repeats Modulate Transcription Factor Activity
Repetitive Sequences, Amino Acid
0301 basic medicine
Saccharomyces cerevisiae Proteins
TANDEM REPEATS
Glutamine
Molecular Sequence Data
Saccharomyces cerevisiae
Article
SACCHAROMYCES-CEREVISIAE
03 medical and health sciences
POLYQ PROTEINS
Gene Expression Regulation, Fungal
POLYGLUTAMINE EXPANSION
YEAST
Protein Interaction Domains and Motifs
PROMOTER NUCLEOSOMES
DNA, Fungal
Molecular Biology
GENE-EXPRESSION
Base Sequence
Protein Stability
BIOFILM FORMATION
Biology and Life Sciences
Cell Biology
CYC8-TUP1 COREPRESSOR
Repressor Proteins
Solubility
PROTEIN HOMEOSTASIS
DOI:
10.1016/j.molcel.2015.07.003
Publication Date:
2015-08-06T20:57:57Z
AUTHORS (12)
ABSTRACT
Excessive expansions of glutamine (Q)-rich repeats in various human proteins are known to result in severe neurodegenerative disorders such as Huntington's disease and several ataxias. However, the physiological role of these repeats and the consequences of more moderate repeat variation remain unknown. Here, we demonstrate that Q-rich domains are highly enriched in eukaryotic transcription factors where they act as functional modulators. Incremental changes in the number of repeats in the yeast transcriptional regulator Ssn6 (Cyc8) result in systematic, repeat-length-dependent variation in expression of target genes that result in direct phenotypic changes. The function of Ssn6 increases with its repeat number until a certain threshold where further expansion leads to aggregation. Quantitative proteomic analysis reveals that the Ssn6 repeats affect its solubility and interactions with Tup1 and other regulators. Thus, Q-rich repeats are dynamic functional domains that modulate a regulator's innate function, with the inherent risk of pathogenic repeat expansions.
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CITATIONS (111)
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