Sun Yi, Shestakova Anna, Hunt Lauren, Sehgal Siddharth, Lupashin Vladimir, Storrie Brian
Department of Physiology and Biophysics, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Mol Biol Cell. 2007 Oct;18(10):4129-42. doi: 10.1091/mbc.e07-01-0080. Epub 2007 Aug 15.
We used multiple approaches to investigate the role of Rab6 relative to Zeste White 10 (ZW10), a mitotic checkpoint protein implicated in Golgi/endoplasmic reticulum (ER) trafficking/transport, and conserved oligomeric Golgi (COG) complex, a putative tether in retrograde, intra-Golgi trafficking. ZW10 depletion resulted in a central, disconnected cluster of Golgi elements and inhibition of ERGIC53 and Golgi enzyme recycling to ER. Small interfering RNA (siRNA) against RINT-1, a protein linker between ZW10 and the ER soluble N-ethylmaleimide-sensitive factor attachment protein receptor, syntaxin 18, produced similar Golgi disruption. COG3 depletion fragmented the Golgi and produced vesicles; vesicle formation was unaffected by codepletion of ZW10 along with COG, suggesting ZW10 and COG act separately. Rab6 depletion did not significantly affect Golgi ribbon organization. Epistatic depletion of Rab6 inhibited the Golgi-disruptive effects of ZW10/RINT-1 siRNA or COG inactivation by siRNA or antibodies. Dominant-negative expression of guanosine diphosphate-Rab6 suppressed ZW10 knockdown induced-Golgi disruption. No cross-talk was observed between Rab6 and endosomal Rab5, and Rab6 depletion failed to suppress p115 (anterograde tether) knockdown-induced Golgi disruption. Dominant-negative expression of a C-terminal fragment of Bicaudal D, a linker between Rab6 and dynactin/dynein, suppressed ZW10, but not COG, knockdown-induced Golgi disruption. We conclude that Rab6 regulates distinct Golgi trafficking pathways involving two separate protein complexes: ZW10/RINT-1 and COG.
我们采用了多种方法来研究Rab6相对于Zeste White 10(ZW10,一种参与高尔基体/内质网(ER)运输/转运的有丝分裂检查点蛋白)和保守寡聚高尔基体(COG)复合物(一种假定的逆行性高尔基体内部运输中的系链)的作用。ZW10缺失导致高尔基体元件形成中央分离簇,并抑制ERGIC53和高尔基体酶循环回到内质网。针对RINT-1(ZW10与内质网可溶性N-乙基马来酰亚胺敏感因子附着蛋白受体Syntaxin 18之间的蛋白质连接物)的小干扰RNA(siRNA)产生了类似的高尔基体破坏。COG3缺失使高尔基体碎片化并产生囊泡;ZW10与COG共同缺失并不影响囊泡形成,这表明ZW10和COG的作用是分开的。Rab6缺失对高尔基体带的组织没有显著影响。Rab6的上位性缺失抑制了ZW10/RINT-1 siRNA或siRNA或抗体介导的COG失活所产生的高尔基体破坏作用。二磷酸鸟苷-Rab6的显性负性表达抑制了ZW10敲低诱导的高尔基体破坏。未观察到Rab6与内体Rab5之间存在相互作用,并且Rab6缺失未能抑制p115(顺行系链)敲低诱导的高尔基体破坏。Rab6与动力蛋白激活蛋白/dynein之间的连接物Bicaudal D的C末端片段的显性负性表达抑制了ZW10敲低诱导的高尔基体破坏,但未抑制COG敲低诱导的高尔基体破坏。我们得出结论,Rab6调节涉及两个独立蛋白质复合物(ZW10/RINT-1和COG)的不同高尔基体运输途径。