Characterization of a novel phospholipase A_1 family

新型磷脂酶 A_1 家族的表征

• 批准号: 15570165
• 负责人: TANI Katsuko
• 金额: $ 2.05万
• 依托单位: Tokyo University of Pharmacy and Life Science
• 依托单位国家: 日本
• 项目类别: Grant-in-Aid for Scientific Research (C)
• 财政年份: 2003
• 资助国家: 日本
• 起止时间: 2003 至 2004
• 项目状态: 已结题
• 来源: https://kaken.nii.ac.jp/en/grant/KAKENHI-PROJECT-15570165/
• 关键词: vesicular transport; endoplasmic reticulum; Golgi apparatus; phospholipase A_1; phosphatidic acid; ホスホリパーゼA; ホフファチジン酸

Transport vesicles coated with the COPII complex, which is assembled from Sar1p, Sec23p-Sec24p, and Secl3p-Sec31p, are involved in protein export from the endoplasmic reticulum(ER). We previously identified a novel Sec23p-interacting protein, p125, which is only expressed in mammals and exhibits sequence homology with phosphatidic acid-preferring phospholipase A_1 (PA-PLA_1). PA-PLA_1,p125, and KIAA0725p appear to constitute an intracellular phospholipase A_1 family. In this study, we have analyzed the localization of PA-PLA_1 and chimeric proteins comprising p125 and two other members. The function of p125 has also been examined in detail using an RNA interference approach.Our previous study showed that p125 is principally localized in ER exit sites where COPII-coated vesicles are produced, and that KIAA0725p is localized in the Golgi. Localization of PA-PLA_1 was analyzed by immunofluorescence microscopy. The results showed that PA-PLA_1 is exclusively localized in the cytosol, differing from that of p125 or KIAA0725p. A chimeric protein composed of the N-terminal region of p125 and KIAA0725p was localized in ER exit sites, but one composed of the N-terminal region of p125 and PA-PLA_1 was in cytosol, indicating that for localization to ER exit sites, the p125-specific N-terminal region is critical, and that the putative lipase domain is interchangeable with KIAA0725p but not with PA-PLA_1. To gain an insight into the function of p125, p125 mRNA was targeted for degradation by RNAi. In p125-depleted cells, the organization of ER exit sites was affected. The structure of the cis-Golgi compartment was also substantially disturbed, whereas the medial-Golgi was not. VSV-G Protein export from the ER occurred without a significant delay in p125-depleted cells. These results suggest that p125 is a mammalian-specific component of ER exit sites and participates in the organization of this compartment.

由Sar1p、Sec23p-Sec24p和Secl3p-Sec31p组装而成的COPII复合体包裹着运输小泡，参与内质网(ER)的蛋白质输出。我们以前发现了一个新的Sec23p相互作用蛋白p125，它只在哺乳动物中表达，与磷脂酸偏好磷脂酶A_1(PA-PLA1)具有序列同源性。PA-PLA1、p125和KIAA0725p似乎构成了胞内磷脂酶A_1家族。在本研究中，我们分析了PA-PLA1和由p125和另外两个成员组成的嵌合蛋白的定位。我们以前的研究表明，p125主要定位于产生COPII包被囊泡的内质网出口部位，KIAA0725p定位于高尔基体。免疫荧光显微镜分析PA-PLA1的定位。结果表明，PA-PLA1不同于p125或KIAA0725p，仅定位于胞浆中。由p125和KIAA0725p的N端区域组成的嵌合蛋白定位于ER出口部位，而由p125和PA-PLA1的N端区域组成的嵌合蛋白位于胞浆中，这表明p125特异的N端区域对于定位到ER出口部位是关键的，推测的脂肪酶结构域可以与KIAA0725p互换，但不能与PA-PLA1互换。为了深入了解p125的功能，RNAi将p125mRNA定位为降解的目标。在p125缺失的细胞中，内质网退出部位的组织受到影响。顺式高尔基体室的结构也受到了很大的干扰，而内侧高尔基体室则没有。在p125缺失的细胞中，VSV-G蛋白从内质网输出没有明显的延迟。这些结果表明，p125是内质网出口部位的哺乳动物特有的成分，并参与了这个隔室的组织。

项目成果

NVL2 is a nucleolar AAA-ATPase that interacts with ribosomal protein L5 through its nucleolar localization sequence.

• DOI: 10.1091/mbc.e04-08-0692
• 发表时间: 2004-10
• 期刊: Molecular biology of the cell
• 影响因子: 3.3
• 作者: M. Nagahama;Y. Hara;Akihiro Seki;Takeshi Yamazoe;Yumiko Kawate;T. Shinohara;K. Hatsuzawa;K. Tani-K.

新規ホスホリパーゼA_1ファミリーの多様な機能

新型磷脂酶A_1家族的多种功能

• 发表时间: 2004
• 期刊: 生化学 76
• 作者: Nagahama;M. et al.;谷 佳津子
• 通讯作者: 谷 佳津子

Hirose, H. et al.: "Implication of ZW1O in membrane trafficking between the endoplasmic reticulum and Golgi"EMBO J.. (In press). (2004)

Hirose, H. 等人：“ZW1O 在内质网和高尔基体之间的膜运输中的意义”EMBO J..（正在出版）。

Kawase, k. et al.: "Gaf-1b is an alternative splice variant of Gaf-1/Rip11."Biophys.Biochem.Res.Commun.. 303. 1042-1046 (2003)

川濑，K.

Identification of B cell adaptor for PI3-kinase (BCAP) as an Ab1 interactor 1-regulated substrate of Ab1 kinases.

鉴定 PI3 激酶 (BCAP) 的 B 细胞接头作为 Ab1 激酶的 Ab1 相互作用子 1 调节底物。

• 发表时间: 2005
• 期刊: FEBS Letters (In press)
• 作者: Maruoka;M. et al.
• 通讯作者: M. et al.