6PY8

Crystal structure of the RBPJ-NOTCH1-NRARP ternary complex bound to DNA

6PY8 の概要

• エントリーDOI: 10.2210/pdb6py8/pdb
• 分子名称: Notch-regulated ankyrin repeat-containing protein, DNA, Recombining binding protein suppressor of hairless, ... (5 entities in total)
• 機能のキーワード: notch1, nrarp, rbpj, dna binding protein, dna binding protein-dna complex, dna binding protein/dna
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 10
• 化学式量合計: 226373.81

構造登録者

Jarrett, S.M.,Seegar, T.C.M.,Blacklow, S.C. (登録日: 2019-07-29, 公開日: 2019-08-14, 最終更新日: 2023-10-11)

主引用文献

Jarrett, S.M.,Seegar, T.C.M.,Andrews, M.,Adelmant, G.,Marto, J.A.,Aster, J.C.,Blacklow, S.C.
Extension of the Notch intracellular domain ankyrin repeat stack by NRARP promotes feedback inhibition of Notch signaling.
Sci.Signal., 12:-, 2019

PubMed Abstract: Canonical Notch signaling relies on regulated proteolysis of the receptor Notch to generate a nuclear effector that induces the transcription of Notch-responsive genes. In higher organisms, one Notch-responsive gene that is activated in many different cell types encodes the Notch-regulated ankyrin repeat protein (NRARP), which acts as a negative feedback regulator of Notch responses. Here, we showed that NRARP inhibited the growth of Notch-dependent T cell acute lymphoblastic leukemia (T-ALL) cell lines and bound directly to the core Notch transcriptional activation complex (NTC), requiring both the transcription factor RBPJ and the Notch intracellular domain (NICD), but not Mastermind-like proteins or DNA. The crystal structure of an NRARP-NICD1-RBPJ-DNA complex, determined to 3.75 Å resolution, revealed that the assembly of NRARP-NICD1-RBPJ complexes relied on simultaneous engagement of RBPJ and NICD1, with the three ankyrin repeats of NRARP extending the Notch1 ankyrin repeat stack. Mutations at the NRARP-NICD1 interface disrupted entry of the proteins into NTCs and abrogated feedback inhibition in Notch signaling assays in cultured cells. Forced expression of NRARP reduced the abundance of NICD in cells, suggesting that NRARP may promote the degradation of NICD. These studies establish the structural basis for NTC engagement by NRARP and provide insights into a critical negative feedback mechanism that regulates Notch signaling.

PubMed: 31690634
DOI: 10.1126/scisignal.aay2369

実験手法

X-RAY DIFFRACTION (3.75 Å)