2020
DOI: 10.14814/phy2.14428
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Actions of Rab27B‐GTPase on mammalian central excitatory synaptic transmission

Abstract: Members of the Rab3 gene family are considered central to membrane trafficking of synaptic vesicles at mammalian central excitatory synapses. Recent evidence, however, indicates that the Rab27B-GTPase, which is highly homologous to the Rab3 family, is also enriched on SV membranes and co-localize with Rab3A and Synaptotagmin at presynaptic terminals. While functional roles of Rab3A have been well-established, little functional information exists on the role of Rab27B in synaptic transmission.Here we report on … Show more

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Cited by 7 publications
(5 citation statements)
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References 59 publications
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“…Among the other candidate genes for the SIT traits, Rab27b is involved in the presynaptic mechanism of long-term potentiation ( 92 ) as well as myelin biogenesis in oligodendrocytes ( 93 ). Ankrd26 is expressed in the arcuate and ventromedial nuclei and in the ependyma Gda , also known as Cypin, in located in the postsynaptic density ( 95 ).…”
Section: Discussionmentioning
confidence: 99%
“…Among the other candidate genes for the SIT traits, Rab27b is involved in the presynaptic mechanism of long-term potentiation ( 92 ) as well as myelin biogenesis in oligodendrocytes ( 93 ). Ankrd26 is expressed in the arcuate and ventromedial nuclei and in the ependyma Gda , also known as Cypin, in located in the postsynaptic density ( 95 ).…”
Section: Discussionmentioning
confidence: 99%
“…For example, a cell type–specific triplet in neurons implicates RAB27B , a guanosine triphosphatase (GTPase) involved in synaptic transmission ( 52 ), in the molecular etiology of MDD. Joint statistical fine-mapping between three traits nominated the SNP rs3764512 as the top candidate, which was located in a neuronal OCR at the gene’s TSS (Fig.…”
Section: Resultsmentioning
confidence: 99%
“…5C, Table S1 ). For example, a cell type specific triplet in neurons implicates RAB27B , a GTPase involved in synaptic transmission ( 33 ), in the molecular etiology of MDD. Joint statistical fine-mapping between three traits nominated the SNP rs3764512 as the top candidate, which is located in a neuronal OCR at the gene’s transcription start site ( Fig.…”
Section: Resultsmentioning
confidence: 99%