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931.
932.
Rong Yu Shiyu Wen Qiaona Wang Congying Wang Liping Zhang Xingxin Wu Jianmei Li Lingdong Kong 《Journal of neurochemistry》2021,157(6):1979-1991
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935.
Steven A. Yukl Shahzada Khan Tsui-Hua Chen Martin Trapecar Frank Wu Guorui Xie Sushama Telwatte Daniel Fulop Alexander R. Pico Gregory M. Laird Kristen D. Ritter Norman G. Jones Chuanyi M. Lu Robert F. Siliciano Nadia R. Roan Jeffrey M. Milush Ma Somsouk Steven G. Deeks Peter W. Hunt Shomyseh Sanjabi 《Journal of virology》2021,95(2)
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938.
Xue Bessie Su Menglu Wang Claudia Schaffner Olga O. Nerusheva Dean Clift Christos Spanos David A. Kelly Michael Tatham Andreas Wallek Yehui Wu Juri Rappsilber A. Arockia Jeyaprakash Zuzana Storchova Ronald T. Hay Adle L. Marston 《The Journal of cell biology》2021,220(7)
During mitosis, sister chromatids attach to microtubules from opposite poles, called biorientation. Sister chromatid cohesion resists microtubule forces, generating tension, which provides the signal that biorientation has occurred. How tension silences the surveillance pathways that prevent cell cycle progression and correct erroneous kinetochore–microtubule attachments remains unclear. Here we show that SUMOylation dampens error correction to allow stable sister kinetochore biorientation and timely anaphase onset. The Siz1/Siz2 SUMO ligases modify the pericentromere-localized shugoshin (Sgo1) protein before its tension-dependent release from chromatin. Sgo1 SUMOylation reduces its binding to protein phosphatase 2A (PP2A), and weakening of this interaction is important for stable biorientation. Unstable biorientation in SUMO-deficient cells is associated with persistence of the chromosome passenger complex (CPC) at centromeres, and SUMOylation of CPC subunit Bir1 also contributes to timely anaphase onset. We propose that SUMOylation acts in a combinatorial manner to facilitate dismantling of the error correction machinery within pericentromeres and thereby sharpen the metaphase–anaphase transition. 相似文献
939.
Fang Chen Bing Yan Jie Ren Rui Lyu Yanfang Wu Yuting Guo Dong Li Hong Zhang Junjie Hu 《The Journal of cell biology》2021,220(5)
Lipid droplets (LDs) are critical for lipid storage and energy metabolism. LDs form in the endoplasmic reticulum (ER). However, the molecular basis for LD biogenesis remains elusive. Here, we show that fat storage–inducing transmembrane protein 2 (FIT2) interacts with ER tubule-forming proteins Rtn4 and REEP5. The association is mainly transmembrane domain based and stimulated by oleic acid. Depletion of ER tubule-forming proteins decreases the number and size of LDs in cells and Caenorhabditis elegans, mimicking loss of FIT2. Through cytosolic loops, FIT2 binds to cytoskeletal protein septin 7, an interaction that is also required for normal LD biogenesis. Depletion of ER tubule-forming proteins or septins delays nascent LD formation. In addition, FIT2-interacting proteins are up-regulated during adipocyte differentiation, and ER tubule-forming proteins, septin 7, and FIT2 are transiently enriched at LD formation sites. Thus, FIT2-mediated nascent LD biogenesis is facilitated by ER tubule-forming proteins and septins. 相似文献
940.
Yanyan Cong Haibo Wu Xuejiao Bian Qin Xie Qifeng Lyu Junqi Cui Lun Suo Yanping Kuang 《Journal of cellular physiology》2021,236(2):1043-1053
Ptk2b has been found playing critical roles in oocyte maturation and subsequent fertilization in vitro. But what is the exact in vivo function in reproduction still elusive. Here, by constructing Ptk2b mutant mice, we found Ptk2b was not essential for mice fertility, unexpectedly, contrary to previously reported in vitro findings, we found Ptk2b ablation significantly improved female fecundity. Follicle counting indicated that the number of primordial follicles and growing follicles in matured mice was significantly increased in the absence of Ptk2b, whereas the primordial follicle formation showed no defects. We also found this regulation was in an autophosphorylation independent pathway, as autophosphorylation site mutant mice (PTK2BY402F) show no phenotype in female fertility. Further biochemistry studies revealed that Ptk2b ablation promotes folliculogenesis via Erk pathway mediate follicle survival. Together, we found a novel biological function of Ptk2b in folliculogenesis, which could be potentially used as a therapeutic target for corresponding infertility. 相似文献