Wang Songyu, Tukachinsky Hanna, Romano Fabian B, Rapoport Tom A
Howard Hughes Medical Institute, Harvard Medical School, Boston, United States.
Department of Cell Biology, Harvard Medical School, Boston, United States.
Elife. 2016 Sep 13;5:e18605. doi: 10.7554/eLife.18605.
In higher eukaryotes, the endoplasmic reticulum (ER) contains a network of membrane tubules, which transitions into sheets during mitosis. Network formation involves curvature-stabilizing proteins, including the reticulons (Rtns), as well as the membrane-fusing GTPase atlastin (ATL) and the lunapark protein (Lnp). Here, we have analyzed how these proteins cooperate. ATL is needed to not only form, but also maintain, the ER network. Maintenance requires a balance between ATL and Rtn, as too little ATL activity or too high Rtn4a concentrations cause ER fragmentation. Lnp only affects the abundance of three-way junctions and tubules. We suggest a model in which ATL-mediated fusion counteracts the instability of free tubule ends. ATL tethers and fuses tubules stabilized by the Rtns, and transiently sits in newly formed three-way junctions. Lnp subsequently moves into the junctional sheets and forms oligomers. Lnp is inactivated by mitotic phosphorylation, which contributes to the tubule-to-sheet conversion of the ER.
在高等真核生物中,内质网(ER)包含一个膜性小管网络,该网络在有丝分裂期间会转变为片层结构。网络形成涉及曲率稳定蛋白,包括网织蛋白(Rtns),以及膜融合GTP酶atlastin(ATL)和月形蛋白(Lnp)。在此,我们分析了这些蛋白如何协同作用。ATL不仅是形成内质网网络所必需的,也是维持该网络所必需的。维持需要ATL和Rtn之间的平衡,因为ATL活性过低或Rtn4a浓度过高都会导致内质网碎片化。Lnp仅影响三岔路口和小管的丰度。我们提出了一个模型,其中ATL介导的融合抵消了游离小管末端的不稳定性。ATL束缚并融合由Rtns稳定的小管,并短暂地位于新形成的三岔路口。随后Lnp进入交界片层并形成寡聚体。Lnp通过有丝分裂磷酸化而失活,这有助于内质网从小管向片层的转变。