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Rab-like small GTPases in the regulation of ciliary Bardet-Biedl syndrome (BBS) complex transport.
Yan, Xiumin; Shen, Yidong.
Afiliação
  • Yan X; Ministry of Education-Shanghai Key Laboratory of Children's Environmental Health, Institute of Early Life Health, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, China.
  • Shen Y; State Key Laboratory of Cell Biology, Shanghai Institute of Biochemistry and Cell Biology, Center for Excellence in Molecular Cell Science, Chinese Academy of Sciences, Shanghai, China.
FEBS J ; 289(23): 7359-7367, 2022 12.
Article em En | MEDLINE | ID: mdl-34655445
ABSTRACT
Primary cilia, microtubule-based hair-like structures protruding from most cells, contain membranes enriched in signaling molecules and function as sensory and regulatory organelles critical for development and tissue homeostasis. Intraflagellar transport (IFT), cilia-specific bidirectional transport, is required for the assembly, maintenance, and function of cilia. BBSome, the coat complex, acts as the adaptor between the IFT complex and membrane proteins and is therefore essential for establishing the specific compartmentalization of signaling molecules in the cilia. Recent findings have revealed that three ciliary Rab-like small GTPases, IFT27, IFT22, and Rabl2, play critical regulatory roles in ciliary BBSome transport. In this review, we provide an overview of these three Rab-like small GTPases and their relationship with BBSome.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Bardet-Biedl / Proteínas Monoméricas de Ligação ao GTP Limite: Humans Idioma: En Revista: FEBS J Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Bardet-Biedl / Proteínas Monoméricas de Ligação ao GTP Limite: Humans Idioma: En Revista: FEBS J Ano de publicação: 2022 Tipo de documento: Article