The Structure of Importin-ß Bound to SREBP-2: Nuclear Import of a Transcription Factor

The sterol regulatory element–binding protein 2 (SREBP-2), a nuclear transcription factor that is essential for cholesterol metabolism, enters the nucleus through a direct interaction of its helix-loop-helix leucine zipper domain with importin-β. We show the crystal structure of importin-β complexed...

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Veröffentlicht in:Science (American Association for the Advancement of Science) 2003-11, Vol.302 (5650), p.1571-1575
Hauptverfasser: Lee, Soo Jae, Sekimoto, Toshihiro, Yamashita, Eiki, Nagoshi, Emi, Nakagawa, Atsushi, Imamoto, Naoko, Yoshimura, Masato, Sakai, Hiroaki, Chong, Khoon Tee, Tsukihara, Tomitake, Yoneda, Yoshihiro
Format: Artikel
Sprache:eng ; jpn
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Zusammenfassung:The sterol regulatory element–binding protein 2 (SREBP-2), a nuclear transcription factor that is essential for cholesterol metabolism, enters the nucleus through a direct interaction of its helix-loop-helix leucine zipper domain with importin-β. We show the crystal structure of importin-β complexed with the active form of SREBP-2. Importin-β uses characteristic long helices like a pair of chopsticks to interact with an SREBP-2 dimer. Importin-β changes its conformation to reveal a pseudo-twofold symmetry on its surface structure so that it can accommodate a symmetric dimer molecule. Importin-β may use a similar strategy to recognize other dimeric cargoes.
ISSN:0036-8075
1095-9203
DOI:10.1126/science.1088372