Document Detail


no child left behind encodes a novel chromatin factor required for germline stem cell maintenance in males but not females.
MedLine Citation:
PMID:  21752937     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Male and female germ cells follow distinct developmental paths with respect to germline stem cell (GSC) production and the types of differentiated progeny they produce (sperm versus egg). An essential aspect of germline development is how sexual identity is used to differentially regulate the male and female germ cell genomes to allow for these distinct outcomes. Here, we identify a gene, no child left behind (nclb), that plays very different roles in the male versus female germline in Drosophila. In particular, nclb is required for GSC maintenance in males, but not in females. Male GSCs mutant for nclb are rapidly lost from the niche, and begin to differentiate but cannot complete spermatogenesis. We further find that nclb encodes a member of a new family of conserved chromatin-associated proteins. NCLB interacts with chromatin in a specific manner and is associated with sites of active transcription. Thus, NCLB appears to be a novel chromatin regulator that exhibits very different effects on the male and female germ cell genomes.
Authors:
Abbie L Casper; Kelly Baxter; Mark Van Doren
Related Documents :
7033277 - A specific plaque-forming cell assay for human thyroglobulin antibody-secreting immunoc...
15666787 - Is reduced cell size the mechanism for shrinkage of the adrenal zona reticularis in aging?
8937687 - Thyroid-specific t cells in the wistar rat: 3. induction of anergy by a syngeneic thyro...
2404227 - A review of the proliferative capacity of major salivary glands and the relationship to...
23070517 - The involvement of proliferation and apoptosis in the early human gonad development.
6733467 - Cells in the pretectal olivary nucleus are in the pathway for the direct light reflex o...
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural     Date:  2011-07-13
Journal Detail:
Title:  Development (Cambridge, England)     Volume:  138     ISSN:  1477-9129     ISO Abbreviation:  Development     Publication Date:  2011 Aug 
Date Detail:
Created Date:  2011-07-27     Completed Date:  2011-10-14     Revised Date:  2013-06-28    
Medline Journal Info:
Nlm Unique ID:  8701744     Medline TA:  Development     Country:  England    
Other Details:
Languages:  eng     Pagination:  3357-66     Citation Subset:  IM    
Affiliation:
Biology Department, Johns Hopkins University, Baltimore, MD 21218, USA.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Animals
Chromatin / metabolism*
Chromosomal Proteins, Non-Histone / genetics,  metabolism*
Drosophila Proteins / genetics,  metabolism*
Drosophila melanogaster / cytology,  embryology,  metabolism*
Epigenesis, Genetic
Female
Gene Expression Regulation, Developmental
Male
Mutation
Oogenesis
Ovum / cytology,  metabolism
Spermatogenesis
Spermatozoa / cytology,  metabolism*
Stem Cells / cytology,  metabolism*
Transcription, Genetic
Grant Support
ID/Acronym/Agency:
GM084356/GM/NIGMS NIH HHS; R01 GM084356-04/GM/NIGMS NIH HHS
Chemical
Reg. No./Substance:
0/Chromatin; 0/Chromosomal Proteins, Non-Histone; 0/Drosophila Proteins; 0/no child left behind protein, Drosophila
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Concerted involvement of Cdx/Hox genes and Wnt signaling in morphogenesis of the caudal neural tube ...
Next Document:  Thyroid hormone contributes to the hypolipidemic effect of polyunsaturated fatty acids from fish oil...