BAIT

CLN3

BTS, JNCL
ceroid-lipofuscinosis, neuronal 3
GO Process (30)
GO Function (2)
GO Component (20)

Gene Ontology Molecular Function

Homo sapiens

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

Interaction between Sdo1p and Btn1p in the Saccharomyces cerevisiae model for Batten disease.

Vitiello SP, Benedict JW, Padilla-Lopez S, Pearce DA

Juvenile Batten disease is an autosomal recessive pediatric neurodegenerative disorder caused by mutations in the CLN3 gene. The CLN3 protein primarily resides in the lysosomal membrane, but its function is unknown. We demonstrate that CLN3 interacts with SBDS, the protein mutated in Shwachman-Bodian-Diamond syndrome patients. We demonstrate that this protein-protein interaction is conserved between Btn1p and Sdo1p, the respective yeast ... [more]

Hum. Mol. Genet. Mar. 01, 2010; 19(5);931-42 [Pubmed: 20015955]

Throughput

  • Low Throughput

Curated By

  • BioGRID