RAB34, Member RAS Oncogene Family Proteine (RAB34)

Mouse (Murine) RAB34, Member RAS Oncogene Family (RAB34) Interaktionspartner

1. Loss-of-function mutations in the Rab34 gene lead to defects in the assembly of primary cilia, in the trafficking of proteins to primary cilia and, consequently, to impaired reception of signals from the Hedgehog (zeige SHH Proteine) pathway.

2. Although Rab34 regulates both lysosomal positioning and lysosome to phagosome fusion, the latter effect is not due to the regulation of the cytoplasmic accessibility of lysosomes to phagosomes by Rab34.

3. uncover Rab34/Munc13-2 as a critical part of an alternative Rab7 (zeige RAB7A Proteine)-independent phagosome maturation machinery and lysosome-mediated killing of mycobacteria

4. results have uncovered a novel mechanism for interorganellar trans-regulation of spatial distribution of lysosomes by Golgi-associated Rab34

Human RAB34, Member RAS Oncogene Family (RAB34) Interaktionspartner

1. Rab34 activity is modulated by SopD2 and is required for maturation of the Salmonella containing vacuole.

2. NARR is ubiquitously expressed and resides in nucleoli where it colocalizes with ribosomal DNA gene clusters.

3. MMP19 (zeige MMP19 Proteine) were positively correlated with RAB34.

4. Although Rab34 regulates both lysosomal positioning and lysosome to phagosome fusion, the latter effect is not due to the regulation of the cytoplasmic accessibility of lysosomes to phagosomes by Rab34.

5. Rab36 (zeige RAB36 Proteine) may regulate the spatial distribution of late endosomes and lysosomes through a similar mechanism to Rab34.

6. The data together indicate that RILP (zeige RILP Proteine), as already demonstrated for several other Rab (zeige HRB Proteine) effector proteins, is capable of self-association, thus probably forming a homo-dimer.

7. Data suggest that diacylglycerol-activated hmunc13 serves as an effector of Rab34, mediating lysosome-Golgi trafficking.

8. define Rab34 as a novel member of the secretory pathway acting at the Golgi

9. B coxsackievirus entry depends on occludin (zeige OCLN Proteine) and require the activity of Rab34, Ras, and Rab5 (zeige RAB5A Proteine), GTPases known to regulate macropinocytosis.

10. mechanistic basis for high glucose-induced protein secretion is through interaction of munc13 and rab34, indicating a potentially critical role for this newly described pathway in the pathogenesis of DN.