학술논문

Xist nucleates local protein gradients to propagate silencing across the X chromosome
Document Type
article
Source
Cell. 184(25)
Subject
Biochemistry and Cell Biology
Bioinformatics and Computational Biology
Biological Sciences
Genetics
Underpinning research
1.1 Normal biological development and functioning
Generic health relevance
Animals
Apoptosis Regulatory Proteins
Cell Line
Embryonic Stem Cells
Fibroblasts
Gene Silencing
Humans
Mice
Mitochondrial Proteins
Protein Binding
RNA
Long Noncoding
X Chromosome
X Chromosome Inactivation
RNA-binding proteins
X chromosome inactivation
Xist RNA
biomolecular condensates
chromatin organization
heterochromatin
macromolecular dynamics
quantitative imaging
super-resolution microscopy
supramolecular complexes
Medical and Health Sciences
Developmental Biology
Biological sciences
Biomedical and clinical sciences
Language
Abstract
The lncRNA Xist forms ∼50 diffraction-limited foci to transcriptionally silence one X chromosome. How this small number of RNA foci and interacting proteins regulate a much larger number of X-linked genes is unknown. We show that Xist foci are locally confined, contain ∼2 RNA molecules, and nucleate supramolecular complexes (SMACs) that include many copies of the critical silencing protein SPEN. Aggregation and exchange of SMAC proteins generate local protein gradients that regulate broad, proximal chromatin regions. Partitioning of numerous SPEN molecules into SMACs is mediated by their intrinsically disordered regions and essential for transcriptional repression. Polycomb deposition via SMACs induces chromatin compaction and the increase in SMACs density around genes, which propagates silencing across the X chromosome. Our findings introduce a mechanism for functional nuclear compartmentalization whereby crowding of transcriptional and architectural regulators enables the silencing of many target genes by few RNA molecules.