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OsERdj7 is an ER-resident J-protein involved in ER quality control in rice endosperm
Journal of Plant Physiology ( IF 4.0 ) Pub Date : 2020-02-01 , DOI: 10.1016/j.jplph.2019.153109
Masaru Ohta 1 , Fumio Takaiwa 2
Affiliation  

OsERdj7 is one of six endoplasmic reticulum (ER)-resident J-domain-containing proteins (J-proteins) encoded by the rice genome that acts as a co-chaperone for Hsp70 and is characterized by the presence of two transmembrane domains. It is N-glycosylated and primarily exists in a dimeric form with a molecular mass of 64 kDa. When the microsomal fraction of maturing seeds was treated with alkaline, high salt or detergent compounds, OsERdj7 was solubilized, even in alkaline and high salt environments, indicating that it is not tightly integrated in the ER membrane. Next, to investigate its role during seed maturation, expression of OsERdj7 was specifically downregulated using RNA interference (RNAi) under the control of the endosperm-specific 16 kDa prolamin promoter in transgenic rice. As a result, the unfolded protein response (UPR) was induced in maturing seeds via activation of OsIRE1/OsbZIP50 and ATF6 orthologs, such as OsbZIP39 and OsbZIP60, leading to upregulation of several chaperones and folding enzymes. Furthermore, some prolamins (RM4 and RM9) were retained in the ER lumen in the form of a mesh-like structure without deposition to the inherent ER-derived protein bodies (PB-Is), although major storage protein glutelins were normally transported to protein storage vacuoles (PB-IIs). On the other hand, induction of ER associated degradation (ERAD) increased OsERdj7 expression in transgenic rice seeds in which ERAD related genes were highly expressed. Due to PDIL2-3 and OsHard3 co-immunoprecipitating with OsERdj7 in rice protoplasts, this result implicates OsERdj7 in the translocation of some seed proteins within the ER lumen and in the degradation of misfolded or unfolded proteins.

中文翻译:

OsERdj7 是一种内质网驻留 J 蛋白,参与水稻胚乳内质网质量控制

OsERdj7 是水稻基因组编码的六种内质网 (ER) 驻留 J 结构域蛋白 (J 蛋白) 之一,作为 Hsp70 的共同伴侣,其特征是存在两个跨膜结构域。它是 N-糖基化的,主要以二聚体形式存在,分子量为 64 kDa。当成熟种子的微粒体部分用碱性、高盐或去污剂化合物处理时,即使在碱性和高盐环境中,OsERdj7 也会溶解,表明它没有紧密地整合到 ER 膜中。接下来,为了研究其在种子成熟过程中的作用,在转基因水稻中胚乳特异性 16 kDa 醇溶蛋白启动子的控制下,使用 RNA 干扰 (RNAi) 特异性下调 OsERdj7 的表达。因此,通过激活 OsIRE1/OsbZIP50 和 ATF6 直向同源物,如 OsbZIP39 和 OsbZIP60,在成熟种子中诱导未折叠蛋白反应 (UPR),导致几种分子伴侣和折叠酶的上调。此外,一些醇溶蛋白(RM4 和 RM9)以网状结构的形式保留在 ER 腔中,而没有沉积到固有的 ER 衍生蛋白体 (PB-Is) 中,尽管主要的储存蛋白谷蛋白通常被转运到蛋白质储存液泡 (PB-II)。另一方面,ER 相关降解 (ERAD) 的诱导增加了 ERAD 相关基因高表达的转基因水稻种子中 OsERdj7 的表达。由于 PDIL2-3 和 OsHard3 在水稻原生质体中与 OsERdj7 共免疫沉淀,
更新日期:2020-02-01
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