BAIT
LMN-1
CELE_DY3.2, Lam1, DY3.2
lmn-1 encodes the sole C. elegans nuclear lamin; lmn-1 is an essential gene that is required for a number of nuclear processes, including chromatin organization, cell cycle progression, chromosome segregation, and nuclear pore complex spacing; LMN-1 is also required for nuclear envelope localization of EMR-1/Emerin during early development; LMN-1 localizes to the nuclear periphery of all cell types except sperm, and in embryonic and some adult cells is visible in the nuclear interior; LMN-1 binds mitotic chromosomes and histone H2A in a manner that requires its predicted nuclear localization signal, KRRR.
GO Process (17)
GO Function (2)
GO Component (3)
Gene Ontology Biological Process
- body morphogenesis [IMP]
- cell cycle arrest [IMP]
- determination of adult lifespan [IMP]
- embryo development ending in birth or egg hatching [IMP]
- germ cell development [IMP]
- hermaphrodite genitalia development [IMP]
- locomotion [IMP]
- mitotic nuclear division [IMP]
- nematode larval development [IMP]
- nuclear pore distribution [IMP]
- nucleus organization [IMP]
- positive regulation of cell proliferation [IMP]
- protein localization [IMP]
- regulation of chromosome segregation [IMP]
- regulation of mitotic cell cycle [IMP]
- reproduction [IMP]
- striated muscle myosin thick filament assembly [IMP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Caenorhabditis elegans
PREY
ZTF-8
CELE_ZC395.8, ZC395.8
Zinc finger putative Transcription Factor family
GO Process (3)
GO Function (0)
GO Component (0)
Gene Ontology Biological Process
Caenorhabditis elegans
Two-hybrid
Bait protein expressed as a DNA binding domain (DBD) fusion and prey expressed as a transcriptional activation domain (TAD) fusion and interaction measured by reporter gene activation.
Publication
Extensive rewiring and complex evolutionary dynamics in a C. elegans multiparameter transcription factor network.
Gene duplication results in two identical paralogs that diverge through mutation, leading to loss or gain of interactions with other biomolecules. Here, we comprehensively characterize such network rewiring for C. elegans transcription factors (TFs) within and across four newly delineated molecular networks. Remarkably, we find that even highly similar TFs often have different interaction degrees and partners. In addition, we find that ... [more]
Mol. Cell Jul. 11, 2013; 51(1);116-27 [Pubmed: 23791784]
Throughput
- High Throughput
Curated By
- BioGRID