Sec7 regulatory domains scaffold autoinhibited and active conformations

Author:

Brownfield Bryce A.12,Richardson Brian C.12ORCID,Halaby Steve L.12,Fromme J. Christopher12ORCID

Affiliation:

1. Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853

2. Weill Institute for Cell and Molecular Biology, Cornell University, Ithaca, NY 14853

Abstract

The late stages of Golgi maturation involve a series of sequential trafficking events in which cargo-laden vesicles are produced and targeted to multiple distinct subcellular destinations. Each of these vesicle biogenesis events requires activation of an Arf GTPase by the Sec7/BIG guanine nucleotide exchange factor (GEF). Sec7 localization and activity is regulated by autoinhibition, positive feedback, and interaction with other GTPases. Although these mechanisms have been characterized biochemically, we lack a clear picture of how GEF localization and activity is modulated by these signals. Here, we report the cryogenic electron microscopy structure of full-length Sec7 in its autoinhibited form, revealing the architecture of its multiple regulatory domains. We use functional experiments to determine the basis for autoinhibition and use structural predictions to produce a model for an active conformation of the GEF that is supported empirically. This study therefore elucidates the conformational transition that Sec7 undergoes to become active on the organelle membrane surface.

Funder

HHS | NIH | National Institute of General Medical Sciences

Publisher

Proceedings of the National Academy of Sciences

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