» Articles » PMID: 32255428

Condensin I Subunit Cap-G is Essential for Proper Gene Expression During the Maturation of Post-mitotic Neurons

Overview
Journal Elife
Specialty Biology
Date 2020 Apr 8
PMID 32255428
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

Condensin complexes are essential for mitotic chromosome assembly and segregation during cell divisions, however, little is known about their functions in post-mitotic cells. Here we report a role for the condensin I subunit Cap-G in neurons. We show that, despite not requiring condensin for mitotic chromosome compaction, post-mitotic neurons express Cap-G. Knockdown of Cap-G specifically in neurons (from their birth onwards) results in developmental arrest, behavioural defects, and dramatic gene expression changes, including reduced expression of a subset of neuronal genes and aberrant expression of genes that are not normally expressed in the developing brain. Knockdown of Cap-G in mature neurons results in similar phenotypes but to a lesser degree. Furthermore, we see dynamic binding of Cap-G at distinct loci in progenitor cells and differentiated neurons. Therefore, Cap-G is essential for proper gene expression in neurons and plays an important role during the early stages of neuronal development.

Citing Articles

How Chromatin Motor Complexes Influence the Nuclear Architecture: A Review of Chromatin Organization, Cohesins, and Condensins with a Focus on .

Chawla B, Csankovszki G DNA (Basel). 2024; 4(1):84-103.

PMID: 39726802 PMC: 11671135. DOI: 10.3390/dna4010005.


"Mitotic" kinesin-5 is a dynamic brake for axonal growth.

Lu W, Lee B, Deng H, Lakonishok M, Martin-Blanco E, Gelfand V bioRxiv. 2024; .

PMID: 39314406 PMC: 11419024. DOI: 10.1101/2024.09.12.612721.


Condensin I folds the Caenorhabditis elegans genome.

Das M, Semple J, Haemmerli A, Volodkina V, Scotton J, Gitchev T Nat Genet. 2024; 56(8):1737-1749.

PMID: 39039278 DOI: 10.1038/s41588-024-01832-5.


Condensin-mediated restriction of retrotransposable elements facilitates brain development in Drosophila melanogaster.

Crawford B, Talley M, Russman J, Riddle J, Torres S, Williams T Nat Commun. 2024; 15(1):2716.

PMID: 38548759 PMC: 10978865. DOI: 10.1038/s41467-024-47042-9.


Maintenance of neuronal fate and transcriptional identity.

Aughey G Biol Open. 2023; 12(6).

PMID: 37272626 PMC: 10259840. DOI: 10.1242/bio.059953.


References
1.
Harding K, White K . Drosophila as a Model for Developmental Biology: Stem Cell-Fate Decisions in the Developing Nervous System. J Dev Biol. 2018; 6(4). PMC: 6315890. DOI: 10.3390/jdb6040025. View

2.
Hocquet C, Robellet X, Modolo L, Sun X, Burny C, Cuylen-Haering S . Condensin controls cellular RNA levels through the accurate segregation of chromosomes instead of directly regulating transcription. Elife. 2018; 7. PMC: 6173581. DOI: 10.7554/eLife.38517. View

3.
Cobbe N, Savvidou E, Heck M . Diverse mitotic and interphase functions of condensins in Drosophila. Genetics. 2005; 172(2):991-1008. PMC: 1456240. DOI: 10.1534/genetics.105.050567. View

4.
Schuster A, Sarvepalli K, Murphy E, Longworth M . Condensin II subunit dCAP-D3 restricts retrotransposon mobilization in Drosophila somatic cells. PLoS Genet. 2013; 9(10):e1003879. PMC: 3814330. DOI: 10.1371/journal.pgen.1003879. View

5.
Van Bortle K, Nichols M, Li L, Ong C, Takenaka N, Qin Z . Insulator function and topological domain border strength scale with architectural protein occupancy. Genome Biol. 2014; 15(6):R82. PMC: 4226948. DOI: 10.1186/gb-2014-15-5-r82. View