Details

Autor(en) / Beteiligte

• Chen, Fusheng
• Hasegawa, Hiroshi
• Schmitt-Ulms, Gerold
• Kawarai, Toshitaka
• Bohm, Christopher
• Katayama, Taiichi
• Gu, Yongjun
• Sanjo, Nobuo
• Glista, Michael
• Rogaeva, Ekaterina
• Wakutani, Yosuke
• Pardossi-Piquard, Raphaelle
• Ruan, Xueying
• Tandon, Anurag

Titel

TMP21 is a presenilin complex component that modulates [gamma]-secretase but not [varepsilon]-secretase activity

Ist Teil von

• Nature (London), 2006-04, Vol.440 (7088), p.1208-1212

Ort / Verlag

London: Nature Publishing Group

Erscheinungsjahr

2006

Quelle

Psychology & Behavioral Sciences Collection

Beschreibungen/Notizen

• The presenilin proteins (PS1 and PS2) and their interacting partners nicastrin, aph-1 (refs 4, 5) and pen-2 (ref. 5) form a series of high-molecular-mass, membrane-bound protein complexes that are necessary for gamma-secretase and epsilon-secretase cleavage of selected type 1 transmembrane proteins, including the amyloid precursor protein, Notch and cadherins. Modest cleavage activity can be generated by reconstituting these four proteins in yeast and Spodoptera frugiperda (sf9) cells. However, a critical but unanswered question about the biology of the presenilin complexes is how their activity is modulated in terms of substrate specificity and/or relative activities at the gamma and epsilon sites. A corollary to this question is whether additional proteins in the presenilin complexes might subsume these putative regulatory functions. The hypothesis that additional proteins might exist in the presenilin complexes is supported by the fact that enzymatically active complexes have a mass that is much greater than predicted for a 1:1:1:1 stoichiometric complex (at least 650 kDa observed, compared with about 220 kDa predicted). To address these questions we undertook a search for presenilin-interacting proteins that differentially affected gamma- and epsilon-site cleavage events. Here we report that TMP21, a member of the p24 cargo protein family, is a component of presenilin complexes and differentially regulates gamma-secretase cleavage without affecting epsilon-secretase activity. [PUBLICATION ABSTRACT]