Locomotion defects, together with Pins, regulates heterotrimeric G-protein signaling during Drosophila neuroblast asymmetric divisions
Article Abstract:
Locomotion defects (Loco) interacts and colocalizes with Galphai and, through its GoLoco motif, acts as a guanine nucleotide dissociation inhibitor (GDI) for Galphai. Simultaneous removal of the two Goloco motif proteins results in defects that are essentially indistinguishable from those observed in Gbeta13F or Ggamma1 mutants, suggesting that Loco and Pins act synergistically to release free Gbetagamma in neuroblasts.
Publication Name: Genes & Development
Subject: Biological sciences
ISSN: 0890-9369
Year: 2005
User Contributions:
Comment about this article or add new information about this topic:
Global analysis of alternative splicing differences between humans and chimpanzees
Article Abstract:
Comparative genomics and quantitative microarray profiling are used for the global analysis of alternative splicing differences between humans and chimpanzees. The alternative splicing differences might affect diverse functions including gene expression, signal transduction, cell death, immune defense and susceptibility to diseases.
Publication Name: Genes & Development
Subject: Biological sciences
ISSN: 0890-9369
Year: 2007
User Contributions:
Comment about this article or add new information about this topic:
- Abstracts: A complex of LIN-5 and GPR proteins regulates G protein signaling and spindle function in C. elegans. The Fanconi road to cancer
- Abstracts: COPII-coated vesicle formation reconstituted with purified coat proteins and chemically defined liposomes. Sar1p N-terminal helix initiates membrane curvature and completes the fission of a COPII vesicle
- Abstracts: High-resolution DNA melt curve analysis of the clustered, regularly interspaced short-palindromic-repeat locus of campylobacter jejuni
- Abstracts: FSH directly regulates bone mass. TSH, the bone suppressing hormone. TSH is a negative regulator of skeletal remodeling
- Abstracts: The structure of ClpB: a molecular chaperone that rescues proteins from an aggregated state. Functional siRNAs and miRNAs exhibit strands bias