Literature DB >> 18050416

X-Chromosome dosage compensation.

Barbara J Meyer1.   

Abstract

In mammals, flies, and worms, sex is determined by distinctive regulatory mechanisms that cause males (XO or XY) and females (XX) to differ in their dose of X chromosomes. In each species, an essential X chromosome-wide process called dosage compensation ensures that somatic cells of either sex express equal levels of X-linked gene products. The strategies used to achieve dosage compensation are diverse, but in all cases, specialized complexes are targeted specifically to the X chromosome(s) of only one sex to regulate transcript levels. In C. elegans, this sex-specific targeting of the dosage compensation complex (DCC) is controlled by the same developmental signal that establishes sex, the ratio of X chromosomes to sets of autosomes (X:A signal). Molecular components of this chromosome counting process have been defined. Following a common step of regulation, sex determination and dosage compensation are controlled by distinct genetic pathways. C. elegans dosage compensation is implemented by a protein complex that binds both X chromosomes of hermaphrodites to reduce transcript levels by one-half. The dosage compensation complex resembles the conserved 13S condensin complex required for both mitotic and meiotic chromosome resolution and condensation, implying the recruitment of ancient proteins to the new task of regulating gene expression. Within each C. elegans somatic cell, one of the DCC components also participates in the separate mitotic/meiotic condensin complex. Other DCC components play pivotal roles in regulating the number and distribution of crossovers during meiosis. The strategy by which C. elegans X chromosomes attract the condensin-like DCC is known. Small, well-dispersed X-recognition elements act as entry sites to recruit the dosage compensation complex and to nucleate spreading of the complex to X regions that lack recruitment sites. In this manner, a repressed chromatin state is spread in cis over short or long distances, thus establishing the global, epigenetic regulation of X chromosomes that is maintained throughout the lifetime of hermaphrodites.

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Year:  2005        PMID: 18050416      PMCID: PMC4781388          DOI: 10.1895/wormbook.1.8.1

Source DB:  PubMed          Journal:  WormBook        ISSN: 1551-8507


  43 in total

Review 1.  Condensin and cohesin complexity: the expanding repertoire of functions.

Authors:  Andrew J Wood; Aaron F Severson; Barbara J Meyer
Journal:  Nat Rev Genet       Date:  2010-05-05       Impact factor: 53.242

2.  Broad chromosomal domains of histone modification patterns in C. elegans.

Authors:  Tao Liu; Andreas Rechtsteiner; Thea A Egelhofer; Anne Vielle; Isabel Latorre; Ming-Sin Cheung; Sevinc Ercan; Kohta Ikegami; Morten Jensen; Paulina Kolasinska-Zwierz; Heidi Rosenbaum; Hyunjin Shin; Scott Taing; Teruaki Takasaki; A Leonardo Iniguez; Arshad Desai; Abby F Dernburg; Hiroshi Kimura; Jason D Lieb; Julie Ahringer; Susan Strome; X Shirley Liu
Journal:  Genome Res       Date:  2010-12-22       Impact factor: 9.043

3.  X chromosome repression by localization of the C. elegans dosage compensation machinery to sites of transcription initiation.

Authors:  Sevinc Ercan; Paul G Giresi; Christina M Whittle; Xinmin Zhang; Roland D Green; Jason D Lieb
Journal:  Nat Genet       Date:  2007-02-11       Impact factor: 38.330

Review 4.  Diverse Genome Topologies Characterize Dosage Compensation across Species.

Authors:  William Jordan; Leila E Rieder; Erica Larschan
Journal:  Trends Genet       Date:  2019-02-23       Impact factor: 11.639

Review 5.  Drosophila dosage compensation: a complex voyage to the X chromosome.

Authors:  Marnie E Gelbart; Mitzi I Kuroda
Journal:  Development       Date:  2009-05       Impact factor: 6.868

6.  A single unpaired and transcriptionally silenced X chromosome locally precludes checkpoint signaling in the Caenorhabditis elegans germ line.

Authors:  Aimee Jaramillo-Lambert; JoAnne Engebrecht
Journal:  Genetics       Date:  2009-12-14       Impact factor: 4.562

7.  Condensins and 3D Organization of the Interphase Nucleus.

Authors:  Heather A Wallace; Giovanni Bosco
Journal:  Curr Genet Med Rep       Date:  2013-12-01

8.  MPK-1 ERK controls membrane organization in C. elegans oogenesis via a sex-determination module.

Authors:  Swathi Arur; Mitsue Ohmachi; Matt Berkseth; Sudhir Nayak; David Hansen; David Zarkower; Tim Schedl
Journal:  Dev Cell       Date:  2011-05-17       Impact factor: 12.270

9.  xol-1, the master sex-switch gene in C. elegans, is a transcriptional target of the terminal sex-determining factor TRA-1.

Authors:  Balázs Hargitai; Vera Kutnyánszky; Timothy A Blauwkamp; Attila Steták; Györgyi Csankovszki; Krisztina Takács-Vellai; Tibor Vellai
Journal:  Development       Date:  2009-12       Impact factor: 6.868

10.  Condensins regulate meiotic DNA break distribution, thus crossover frequency, by controlling chromosome structure.

Authors:  David G Mets; Barbara J Meyer
Journal:  Cell       Date:  2009-09-24       Impact factor: 41.582

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