TY - JOUR
T1 - Rab32 subfamily small GTPases
T2 - Pleiotropic Rabs in endosomal trafficking
AU - Ohbayashi, Norihiko
AU - Fukuda, Mitsunori
AU - Kanaho, Yasunori
N1 - Funding Information:
This work was supported by Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan (Grant-in-Aid for Scientific Research (C) JP15K07039 to N. O., Grant-in-Aid for Scientific Research (B) JP15H04367 and Grant-in-Aid for Scientific Research on Innovative Areas JP16H01189 to M. F., and Grant-in-Aid for Scientific Research (A) JP15H02503 to Y. K.) and by the Cosmetology Research Foundation (to N.O.).
PY - 2017/8/1
Y1 - 2017/8/1
N2 - Rab small GTPases, well-known regulators of membrane trafficking pathways in eukaryotic cells, comprise approximately 60 different members in mammals. During the past decade, our understanding of the functions of mammalian Rab32 subfamily members (Rab32 and Rab38) have deepened, especially on the biogenesis of lysosome-related organelles, such as melanosomes, and the protection mechanisms against several pathogenic microbial infections. Endosome-mediated membrane trafficking by Rab32 subfamily members plays pivotal roles in these events. In this review, we provide an overview of the regulatory mechanisms of mammalian Rab32-family members in endosomal trafficking, especially focusing on their GEF, GAP and effector molecules, and describe the latest findings on physiological and pathological functions regulated by these molecules.
AB - Rab small GTPases, well-known regulators of membrane trafficking pathways in eukaryotic cells, comprise approximately 60 different members in mammals. During the past decade, our understanding of the functions of mammalian Rab32 subfamily members (Rab32 and Rab38) have deepened, especially on the biogenesis of lysosome-related organelles, such as melanosomes, and the protection mechanisms against several pathogenic microbial infections. Endosome-mediated membrane trafficking by Rab32 subfamily members plays pivotal roles in these events. In this review, we provide an overview of the regulatory mechanisms of mammalian Rab32-family members in endosomal trafficking, especially focusing on their GEF, GAP and effector molecules, and describe the latest findings on physiological and pathological functions regulated by these molecules.
KW - GAP
KW - GEF
KW - Rab.
KW - lysosome-related organelles
KW - membrane traffic
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U2 - 10.1093/jb/mvx027
DO - 10.1093/jb/mvx027
M3 - Review article
C2 - 28430987
AN - SCOPUS:85029147498
VL - 162
SP - 65
EP - 71
JO - Journal of Biochemistry
JF - Journal of Biochemistry
SN - 0021-924X
IS - 2
ER -