BAIT

PAFAH1B1

LIS1, LIS2, MDCR, MDS, PAFAH
platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa)
Homo sapiens
PREY

DAB1

RP6-239D12.2
Dab, reelin signal transducer, homolog 1 (Drosophila)
GO Process (0)
GO Function (0)
GO Component (0)
Homo sapiens

Reconstituted Complex

An interaction is detected between purified proteins in vitro.

Publication

Interaction of reelin signaling and Lis1 in brain development.

Assadi AH, Zhang G, Beffert U, McNeil RS, Renfro AL, Niu S, Quattrocchi CC, Antalffy BA, Sheldon M, Armstrong DD, Wynshaw-Boris A, Herz J, D'Arcangelo G, Clark GD

Loss-of-function mutations in RELN (encoding reelin) or PAFAH1B1 (encoding LIS1) cause lissencephaly, a human neuronal migration disorder. In the mouse, homozygous mutations in Reln result in the reeler phenotype, characterized by ataxia and disrupted cortical layers. Pafah1b1(+/-) mice have hippocampal layering defects, whereas homozygous mutants are embryonic lethal. Reln encodes an extracellular protein that regulates layer formation by interacting with ... [more]

Nat. Genet. Nov. 01, 2003; 35(3);270-6 [Pubmed: 14578885]

Throughput

  • Low Throughput

Additional Notes

  • assayed using IP (immunoprecipitation) experiments using Dab1 produced by IVTT (in vitro transcription/translation) and Lis1 purified from human cells

Curated By

  • BioGRID