Literature DB >> 22323658

Role of Rab family GTPases and their effectors in melanosomal logistics.

Norihiko Ohbayashi1, Mitsunori Fukuda.   

Abstract

Rab GTPases constitute a family of small GTPases that regulate a variety of membrane trafficking events in all eukaryotic cells by recruiting their specific effector molecules. Recent accumulating evidence indicates that members of the mammalian Rab small GTPase family are involved in certain physiological and pathological processes. In particular, functional impairments of specific Rab proteins, e.g. Rab38 and Rab27A, their regulators or their effectors cause pigmentation disorders in humans and coat colour variations in mice because such impairments cause defects in melanosomal logistics, i.e. defects in melanosome biogenesis and transport. Genetic and biochemical analyses of the gene products responsible for mammalian pigmentation disorders in the past decade have revealed that Rab-mediated endosomal transport systems and melanosome transport systems play crucial roles in the efficient darkening of mammalian hair and skin. In this article, we review current knowledge regarding melanosomal logistics, with particular focus on the roles of Rab small GTPases and their effectors.

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Year:  2012        PMID: 22323658     DOI: 10.1093/jb/mvs009

Source DB:  PubMed          Journal:  J Biochem        ISSN: 0021-924X            Impact factor:   3.387


  25 in total

1.  The Two-pore channel (TPC) interactome unmasks isoform-specific roles for TPCs in endolysosomal morphology and cell pigmentation.

Authors:  Yaping Lin-Moshier; Michael V Keebler; Robert Hooper; Michael J Boulware; Xiaolong Liu; Dev Churamani; Mary E Abood; Timothy F Walseth; Eugen Brailoiu; Sandip Patel; Jonathan S Marchant
Journal:  Proc Natl Acad Sci U S A       Date:  2014-08-25       Impact factor: 11.205

Review 2.  Regulation of autophagy by the Rab GTPase network.

Authors:  X Ao; L Zou; Y Wu
Journal:  Cell Death Differ       Date:  2014-01-17       Impact factor: 15.828

3.  MicroRNA-203 regulates melanosome transport and tyrosinase expression in melanoma cells by targeting kinesin superfamily protein 5b.

Authors:  Shunsuke Noguchi; Minami Kumazaki; Yuki Yasui; Takashi Mori; Nami Yamada; Yukihiro Akao
Journal:  J Invest Dermatol       Date:  2013-07-22       Impact factor: 8.551

4.  The BLOC-3 subunit HPS4 is required for activation of Rab32/38 GTPases in melanogenesis, but its Rab9 activity is dispensable for melanogenesis.

Authors:  Yuta Ohishi; Riko Kinoshita; Soujiro Marubashi; Morié Ishida; Mitsunori Fukuda
Journal:  J Biol Chem       Date:  2019-03-05       Impact factor: 5.157

Review 5.  Bacterial pathogens commandeer Rab GTPases to establish intracellular niches.

Authors:  Mary-Pat Stein; Matthias P Müller; Angela Wandinger-Ness
Journal:  Traffic       Date:  2012-09-13       Impact factor: 6.215

Review 6.  Melanosome transfer: it is best to give and receive.

Authors:  Xufeng Wu; John A Hammer
Journal:  Curr Opin Cell Biol       Date:  2014-03-21       Impact factor: 8.382

7.  Rab from the white shrimp Litopenaeus vannamei: characterization and its regulation upon environmental stress.

Authors:  Lei Wang; Xiao-Rong Wang; Jin Liu; Chu-Xian Chen; Yuan Liu; Wei-Na Wang
Journal:  Ecotoxicology       Date:  2015-05-08       Impact factor: 2.823

Review 8.  Participation of keratinocyte- and fibroblast-derived factors in melanocyte homeostasis, the response to UV, and pigmentary disorders.

Authors:  Parth R Upadhyay; Tina Ho; Zalfa A Abdel-Malek
Journal:  Pigment Cell Melanoma Res       Date:  2021-05-24       Impact factor: 4.693

9.  Fibroblast growth factor signalling controls nervous system patterning and pigment cell formation in Ciona intestinalis.

Authors:  Claudia Racioppi; Ashwani K Kamal; Florian Razy-Krajka; Gennaro Gambardella; Laura Zanetti; Diego di Bernardo; Remo Sanges; Lionel A Christiaen; Filomena Ristoratore
Journal:  Nat Commun       Date:  2014-09-05       Impact factor: 17.694

Review 10.  Cell type-specific Rab32 and Rab38 cooperate with the ubiquitous lysosome biogenesis machinery to synthesize specialized lysosome-related organelles.

Authors:  Jarred J Bultema; Santiago M Di Pietro
Journal:  Small GTPases       Date:  2012-12-17
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