Sharif Mohamed, Greenberg Lydia, Bangs James
Department of Biochemistry, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, 955 Main Street, Buffalo NY 14203.
Current address: Department of Cancer Genetics & Genomics Roswell Park Comprehensive Cancer Center 665 Elm St, Buffalo, NY 14203.
bioRxiv. 2024 Dec 4:2024.12.03.626618. doi: 10.1101/2024.12.03.626618.
Secretory cargos are exported from the ER via COPII coated vesicles that have an inner matrix of Sec23/Sec24 heterotetramers and an outer cage of Sec13/Sec31 heterotetramers. In addition to COPII, Sec13 is part of the nuclear pore complex (NPC) and the regulatory SEA/GATOR complex in eukaryotes, which typically have one Sec13 orthologue. The kinetoplastid parasite has two paralogues: TbSec13.1, an accepted component of both COPII and the NPC, and TbSec13.2. Little is known about TbSec13.2, but others have proposed that it, and its orthologue in the distantly related diplonemid , operate exclusively in the SEA/GATOR complex, and that this represents an evolutionary diversification of function unique to the euglenozoan protists (doi.org/10.1098/rsob.220364). Using RNAi silencing in trypanosomes we show both TbSec13s are essential. Knockdown of each dramatically and equally delays transport of GPI-anchored secretory cargo, indicating roles for both in COPII-mediated trafficking from the ER. Immunofluorescence and proximity labeling studies confirm that both TbSec13.1 and TbSec13.2 co-localize with TbSec24.1 to ER exit sites, and thus are functional components of the COPII machinery. Our findings indicate that TbSec13.2 function is not restricted to the SEA/GATOR complex in trypanosomes.
分泌性货物通过COPII包被的囊泡从内质网输出,这些囊泡具有由Sec23/Sec24异源四聚体组成的内部基质和由Sec13/Sec31异源四聚体组成的外部笼状结构。除了COPII,Sec13还是真核生物中核孔复合体(NPC)和调节性SEA/GATOR复合体的一部分,真核生物通常有一个Sec13直系同源物。动基体寄生虫有两个旁系同源物:TbSec13.1,它是COPII和NPC的公认组成部分,以及TbSec13.2。人们对TbSec13.2了解甚少,但其他人提出,它及其在远缘相关双滴虫中的直系同源物仅在SEA/GATOR复合体中发挥作用,并且这代表了眼虫类原生生物特有的功能进化多样化(doi.org/10.1098/rsob.220364)。我们在锥虫中使用RNAi沉默表明,两个TbSec13都是必需的。对每个基因的敲低都显著且同等程度地延迟了糖基磷脂酰肌醇(GPI)锚定的分泌性货物的运输,表明它们在COPII介导的从内质网的运输中都发挥作用。免疫荧光和邻近标记研究证实,TbSec13.1和TbSec13.2都与TbSec24.