Autophagy最新文献

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Autophagy preserves hematopoietic stem cells by restraining MTORC1-mediated cellular anabolism. 自噬通过抑制MTORC1介导的细胞合成代谢来保存造血干细胞。
IF 14.6 1区 生物学
Autophagy Pub Date : 2024-01-01 Epub Date: 2023-08-23 DOI: 10.1080/15548627.2023.2247310
Mariana Borsa, Sandrine Obba, Felix C Richter, Hanlin Zhang, Thomas Riffelmacher, Joana Carrelha, Ghada Alsaleh, Sten Eirik W Jacobsen, Anna Katharina Simon
{"title":"Autophagy preserves hematopoietic stem cells by restraining MTORC1-mediated cellular anabolism.","authors":"Mariana Borsa, Sandrine Obba, Felix C Richter, Hanlin Zhang, Thomas Riffelmacher, Joana Carrelha, Ghada Alsaleh, Sten Eirik W Jacobsen, Anna Katharina Simon","doi":"10.1080/15548627.2023.2247310","DOIUrl":"10.1080/15548627.2023.2247310","url":null,"abstract":"<p><p>Adult stem cells are long-lived and quiescent with unique metabolic requirements. Macroautophagy/autophagy is a fundamental survival mechanism that allows cells to adapt to metabolic changes by degrading and recycling intracellular components. Here we address why autophagy depletion leads to a drastic loss of the stem cell compartment. Using inducible deletion of autophagy specifically in adult hematopoietic stem cells (HSCs) and in mice chimeric for autophagy-deficient and normal HSCs, we demonstrate that the stem cell loss is cell-intrinsic. Mechanistically, autophagy-deficient HSCs showed higher expression of several amino acid transporters (AAT) when compared to autophagy-competent cells, resulting in increased amino acid (AA) uptake. This was followed by sustained MTOR (mechanistic target of rapamycin) activation, with enlarged cell size, glucose uptake and translation, which is detrimental to the quiescent HSCs. MTOR inhibition by rapamycin treatment <i>in vivo</i> was able to rescue autophagy-deficient HSC loss and bone marrow failure and resulted in better reconstitution after transplantation. Our results suggest that targeting MTOR may improve aged stem cell function, promote reprogramming and stem cell transplantation.<b>List of abbreviations:</b> 5FU: fluoracil; AA: amino acids; AKT/PKB: thymoma viral proto-oncogene 1; ATF4: activating transcription factor 4; BafA: bafilomycin A<sub>1</sub>; BM: bone marrow; EIF2: eukaryotic initiation factor 2; EIF4EBP1/4EBP1: eukaryotic translation initiation factor 4E binding protein 1; KIT/CD117/c-Kit: KIT proto-oncogene receptor tyrosine kinase; HSCs: hematopoietic stem cells; HSPCs: hematopoietic stem and progenitor cells; Kyn: kynurenine; LSK: lineage<sup>-</sup> (Lin<sup>-</sup>), LY6A/Sca-1<sup>+</sup>, KIT/c-Kit/CD117<sup>+</sup>; LY6A/Sca-1: lymphocyte antigen 6 family member A; MTOR: mechanistic target of rapamycin kinase; MTORC1: MTOR complex 1; MTORC2: MTOR complex 2; OPP: O-propargyl-puromycin; PI3K: phosphoinositide 3-kinase; poly(I:C): polyinosinic:polycytidylic acid; RPS6/S6: ribosomal protein S6; tam: tamoxifen; TCA: tricarboxylic acid; TFEB: transcription factor EB; PTPRC/CD45: Protein Tyrosine Phosphatase Receptor Type C, CD45 antigen.</p>","PeriodicalId":8722,"journal":{"name":"Autophagy","volume":" ","pages":"45-57"},"PeriodicalIF":14.6,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10761185/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10116425","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mammalian phagophores with finger-like shapes emerge from recycling endosomes 哺乳动物具有指状形状的吞噬细胞从循环内体中出现
IF 13.3 1区 生物学
Autophagy Pub Date : 2023-12-14 DOI: 10.1080/15548627.2023.2293439
Claudia Puri, David C Rubinsztein
{"title":"Mammalian phagophores with finger-like shapes emerge from recycling endosomes","authors":"Claudia Puri, David C Rubinsztein","doi":"10.1080/15548627.2023.2293439","DOIUrl":"https://doi.org/10.1080/15548627.2023.2293439","url":null,"abstract":"Autophagosomes are double-membraned vesicles that engulf cytoplasmic contents, which are ultimately degraded after autophagosome-lysosome fusion. The prevailing view, largely inferred from EM-based...","PeriodicalId":8722,"journal":{"name":"Autophagy","volume":"17 1","pages":""},"PeriodicalIF":13.3,"publicationDate":"2023-12-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138684641","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Senecavirus a induces mitophagy to promote self-replication through direct interaction of 2C protein with K27-linked ubiquitinated TUFM catalyzed by RNF185 森纳卡病毒 a 通过 2C 蛋白与 RNF185 催化的 K27 链接泛素化 TUFM 的直接相互作用,诱导有丝分裂以促进自我复制
IF 13.3 1区 生物学
Autophagy Pub Date : 2023-12-12 DOI: 10.1080/15548627.2023.2293442
Meirong Chen, Xin Zhang, Fanshu Kong, Peng Gao, Xinna Ge, Lei Zhou, Jun Han, Xin Guo, Yongning Zhang, Hanchun Yang
{"title":"Senecavirus a induces mitophagy to promote self-replication through direct interaction of 2C protein with K27-linked ubiquitinated TUFM catalyzed by RNF185","authors":"Meirong Chen, Xin Zhang, Fanshu Kong, Peng Gao, Xinna Ge, Lei Zhou, Jun Han, Xin Guo, Yongning Zhang, Hanchun Yang","doi":"10.1080/15548627.2023.2293442","DOIUrl":"https://doi.org/10.1080/15548627.2023.2293442","url":null,"abstract":"Senecavirus A (SVA) is a newly emerging picornavirus associated with swine vesicular lesions and neonatal mortality, threatening the global pig industry. Despite sustained efforts, the molecular me...","PeriodicalId":8722,"journal":{"name":"Autophagy","volume":"39 1","pages":""},"PeriodicalIF":13.3,"publicationDate":"2023-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138579794","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The hookup model of the HOPS complex in autophagosome-lysosome fusion 自噬体-溶酶体融合过程中的 HOPS 复合物挂钩模型
IF 13.3 1区 生物学
Autophagy Pub Date : 2023-12-11 DOI: 10.1080/15548627.2023.2291938
Shen Zhang, Linsen Li, Xiaoxia Liu, Qing Zhong
{"title":"The hookup model of the HOPS complex in autophagosome-lysosome fusion","authors":"Shen Zhang, Linsen Li, Xiaoxia Liu, Qing Zhong","doi":"10.1080/15548627.2023.2291938","DOIUrl":"https://doi.org/10.1080/15548627.2023.2291938","url":null,"abstract":"Macroautophagy/autophagy is a highly conserved process that involves the degradation of proteins, damaged organelles, and other cytoplasmic macromolecules. Autophagosome-lysosome fusion is critical...","PeriodicalId":8722,"journal":{"name":"Autophagy","volume":"21 1","pages":""},"PeriodicalIF":13.3,"publicationDate":"2023-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138579845","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
LTN1 promotes RLR degradation to inhibit immune response to RNA virus through the ESCRT pathway LTN1 通过 ESCRT 途径促进 RLR 降解,抑制对 RNA 病毒的免疫反应
IF 13.3 1区 生物学
Autophagy Pub Date : 2023-12-07 DOI: 10.1080/15548627.2023.2291939
Fei Qin, Baoshan Cai, Peng Wang, Runyu Cao, Yuling Zhang, Hongling Wen, Yi Zheng, Wei Zhao, Chengjiang Gao, Bingyu Liu
{"title":"LTN1 promotes RLR degradation to inhibit immune response to RNA virus through the ESCRT pathway","authors":"Fei Qin, Baoshan Cai, Peng Wang, Runyu Cao, Yuling Zhang, Hongling Wen, Yi Zheng, Wei Zhao, Chengjiang Gao, Bingyu Liu","doi":"10.1080/15548627.2023.2291939","DOIUrl":"https://doi.org/10.1080/15548627.2023.2291939","url":null,"abstract":"The excessive activation of immune responses will trigger autoimmune diseases or inflammatory injury. The endosomal sorting complexes required for transport (ESCRT) system can capture and mediate u...","PeriodicalId":8722,"journal":{"name":"Autophagy","volume":"8 1","pages":""},"PeriodicalIF":13.3,"publicationDate":"2023-12-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138554653","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The constructive and destructive impact of autophagy on both genders' reproducibility, a comprehensive review. 自噬对两性再现性的建设性和破坏性影响,全面综述。
IF 14.6 1区 生物学
Autophagy Pub Date : 2023-12-01 Epub Date: 2023-07-28 DOI: 10.1080/15548627.2023.2238577
Mohammad Samare-Najaf, Asma Neisy, Ali Samareh, Delaram Moghadam, Navid Jamali, Reza Zarei, Fatemeh Zal
{"title":"The constructive and destructive impact of autophagy on both genders' reproducibility, a comprehensive review.","authors":"Mohammad Samare-Najaf, Asma Neisy, Ali Samareh, Delaram Moghadam, Navid Jamali, Reza Zarei, Fatemeh Zal","doi":"10.1080/15548627.2023.2238577","DOIUrl":"10.1080/15548627.2023.2238577","url":null,"abstract":"<p><p>Reproduction is characterized by a series of massive renovations at molecular, cellular, and tissue levels. Recent studies have strongly tended to reveal the involvement of basic molecular pathways such as autophagy, a highly conserved eukaryotic cellular recycling, during reproductive processes. This review comprehensively describes the current knowledge, updated to September 2022, of autophagy contribution during reproductive processes in males including spermatogenesis, sperm motility and viability, and male sex hormones and females including germ cells and oocytes viability, ovulation, implantation, fertilization, and female sex hormones. Furthermore, the consequences of disruption in autophagic flux on the reproductive disorders including oligospermia, azoospermia, asthenozoospermia, teratozoospermia, globozoospermia, premature ovarian insufficiency, polycystic ovarian syndrome, endometriosis, and other disorders related to infertility are discussed as well.<b>Abbreviations:</b> AKT/protein kinase B: AKT serine/threonine kinase; AMPK: AMP-activated protein kinase; ATG: autophagy related; E<sub>2:</sub> estrogen; EDs: endocrine disruptors; ER: endoplasmic reticulum; FSH: follicle stimulating hormone; FOX: forkhead box; GCs: granulosa cells; HIF: hypoxia inducible factor; IVF: in vitro fertilization; IVM: in vitro maturation; LCs: Leydig cells; LDs: lipid droplets; LH: luteinizing hormone; LRWD1: leucine rich repeats and WD repeat domain containing 1; MAP1LC3: microtubule associated protein 1 light chain 3; MAPK: mitogen-activated protein kinase; MTOR: mechanistic target of rapamycin kinase; NFKB/NF-kB: nuclear factor kappa B; P<sub>4</sub>: progesterone; PCOS: polycystic ovarian syndrome; PDLIM1: PDZ and LIM domain 1; PI3K: phosphoinositide 3-kinase; PtdIns3P: phosphatidylinositol-3-phosphate; PtdIns3K: class III phosphatidylinositol 3-kinase; POI: premature ovarian insufficiency; ROS: reactive oxygen species; SCs: Sertoli cells; SQSTM1/p62: sequestosome 1; TSGA10: testis specific 10; TST: testosterone; VCP: vasolin containing protein.</p>","PeriodicalId":8722,"journal":{"name":"Autophagy","volume":" ","pages":"3033-3061"},"PeriodicalIF":14.6,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10621263/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10209596","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Activated STING1 rides the Rafeesome. 激活的STING1乘坐Rafeesome。
IF 14.6 1区 生物学
Autophagy Pub Date : 2023-12-01 Epub Date: 2023-08-06 DOI: 10.1080/15548627.2023.2240154
Yaping Han, Jianfei Zheng, Liang Ge
{"title":"Activated STING1 rides the Rafeesome.","authors":"Yaping Han, Jianfei Zheng, Liang Ge","doi":"10.1080/15548627.2023.2240154","DOIUrl":"10.1080/15548627.2023.2240154","url":null,"abstract":"<p><p>Over the past decade, accumulated studies have reported the presence of non-canonical macroautophagy/autophagy characterized by the shared usage of the autophagy machinery and distinct components that function in multiple scenarios but do not involve lysosomal degradation. One type of non-canonical autophagy is secretory autophagy, which facilitates the secretion of various cargoes. In a recent work from Gao et al. the ER-membrane protein STING1 has been identified as a novel substrate of secretory autophagy. The secretion of activated STING1 is mediated by its packing into the rafeesome, a newly identified organelle formed upon the fusion of RAB22A-mediated non-canonical autophagosome with an early endosome. Moreover, extracellular vesicles containing activated STING1 induce antitumor immunity in recipient cells, a process potentially promoted by RAB22A.</p>","PeriodicalId":8722,"journal":{"name":"Autophagy","volume":" ","pages":"3230-3233"},"PeriodicalIF":14.6,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10621249/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10302375","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Autophagy contributes to positive feedback regulation of SnRK1 signaling in plants. 自噬有助于植物中SnRK1信号的正反馈调节。
IF 14.6 1区 生物学
Autophagy Pub Date : 2023-12-01 Epub Date: 2023-08-20 DOI: 10.1080/15548627.2023.2247741
Chao Yang, Xibao Li, Jun Zhou, Caiji Gao
{"title":"Autophagy contributes to positive feedback regulation of SnRK1 signaling in plants.","authors":"Chao Yang, Xibao Li, Jun Zhou, Caiji Gao","doi":"10.1080/15548627.2023.2247741","DOIUrl":"10.1080/15548627.2023.2247741","url":null,"abstract":"<p><p>SnRK1 (SNF1-related protein kinase 1) is a plant ortholog of yeast Snf1 and mammalian adenosine monophosphate-activated protein kinase (AMPK) that acts as a positive regulator of macroautophagy/autophagy. However, whether and how the autophagy pathway modulates SnRK1 activity remains elusive. Recently, we identified a clade of plant-specific FLZ (FCS-like zinc finger) proteins as novel ATG8 (autophagy-related 8)-interacting partners in <i>Arabidopsis thaliana</i>. These AtFLZs, which mainly localize on the surface of mitochondria, can inhibit SnRK1 signaling by repressing the T-loop phosphorylation of its catalytic α subunits, thereby negatively regulating carbon starvation-induced autophagy and plant tolerance to energy deprivation. Upon energy starvation, autophagy is activated to mediate the degradation of these AtFLZs, thus relieving their repression of SnRK1. More importantly, the ATG8-FLZ-SnRK1 regulatory axis appears to be functionally conserved during seed plant evolution. These findings highlight the positive role of autophagy in SnRK1 signaling activation under energy-limiting conditions in plants.<b>Abbreviations:</b> ADS, AIMs docking site; AIM, ATG8-interacting motif; AMPK, adenosine monophosphate-activated protein kinase; ATG, autophagy-related; ESCRT, endosomal sorting complexes required for transport; FLZ, FCS-like zinc finger protein; FREE1, FYVE DOMAIN PROTEIN REQUIRED FOR ENDOSOMAL SORTING 1; RAPTOR, REGULATORY-ASSOCIATED PROTEIN OF TOR; Snf1, SUCROSE NON-FERMENTING 1; SnRK1, SNF1-related kinase 1; TOR, TARGET OF RAPAMYCIN.</p>","PeriodicalId":8722,"journal":{"name":"Autophagy","volume":" ","pages":"3248-3250"},"PeriodicalIF":14.6,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10621257/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10387163","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
LC3 conjugation to lipid droplets. LC3与脂滴结合。
IF 14.6 1区 生物学
Autophagy Pub Date : 2023-12-01 Epub Date: 2023-08-23 DOI: 10.1080/15548627.2023.2249390
Mohyeddine Omrane, Thomas J Melia, Abdou Rachid Thiam
{"title":"LC3 conjugation to lipid droplets.","authors":"Mohyeddine Omrane, Thomas J Melia, Abdou Rachid Thiam","doi":"10.1080/15548627.2023.2249390","DOIUrl":"10.1080/15548627.2023.2249390","url":null,"abstract":"<p><p>Macroautophagy/autophagy and lipid droplet (LD) biology are intricately linked, with autophagosome-dependent degradation of LDs in response to different signals. LDs play crucial roles in forming autophagosomes possibly by providing essential lipids and serving as a supportive autophagosome assembly platform at the endoplasmic reticulum (ER)-LD interface. LDs and autophagosomes share common proteins, such as VPS13, ATG2, ZFYVE1/DFCP1, and ATG14, but their dual functions remain poorly understood. In our recent study, we found that prolonged starvation leads to ATG3 localizing to large LDs and lipidating LC3B, revealing a non-canonical autophagic role on LDs. In vitro, ATG3 associates with purified and artificial LDs, and conjugated Atg8-family proteins. In long-term starved cells, only LC3B is found on the specific large LDs, positioned near LC3B-positive membranes that undergo lysosome-mediated acidification. This implies that LD-lipidated LC3B acts as a tethering factor, connecting phagophores to LDs and promoting degradation. Our data also support the notion that certain LD surfaces may function as lipidation stations for LC3B, which may move to nearby sites of autophagosome formation. Overall, our study unveils an unknown non-canonical implication of LDs in autophagy processes.<b>Abbreviation:</b> ATG: autophagy-related enzyme, ATP: adenosine triphosphate, E2 enzyme: ubiquitin-conjugating enzyme, ER: endoplasmic reticulum, LD: lipid droplet, LIR motif: LC3-interacting region, MAP1LC3B/LC3B: microtubule-associated protein 1 light chain 3 beta, PE: phosphatidylethanolamine, PLIN1: perilipin 1, PNPLA2/ATGL: patatin-like phospholipase domain containing 2, SQSTM1/p62: sequestosome 1, VSP13: vacuolar protein sorting 13, ZFYVE1/DFCP1: zinc finger, FYVE domain containing 1.</p>","PeriodicalId":8722,"journal":{"name":"Autophagy","volume":" ","pages":"3251-3253"},"PeriodicalIF":14.6,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10621252/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10060314","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
LIRcentral: a manually curated online database of experimentally validated functional LIR motifs. LIRcentral:一个人工策划的在线数据库,包含实验验证的功能性LIR基序。
IF 13.3 1区 生物学
Autophagy Pub Date : 2023-12-01 Epub Date: 2023-08-02 DOI: 10.1080/15548627.2023.2235851
Agathangelos Chatzichristofi, Vasileios Sagris, Aristos Pallaris, Marios Eftychiou, Ioanna Kalvari, Nicholas Price, Theodosios Theodosiou, Ioannis Iliopoulos, Ioannis P Nezis, Vasilis J Promponas
{"title":"LIRcentral: a manually curated online database of experimentally validated functional LIR motifs.","authors":"Agathangelos Chatzichristofi,&nbsp;Vasileios Sagris,&nbsp;Aristos Pallaris,&nbsp;Marios Eftychiou,&nbsp;Ioanna Kalvari,&nbsp;Nicholas Price,&nbsp;Theodosios Theodosiou,&nbsp;Ioannis Iliopoulos,&nbsp;Ioannis P Nezis,&nbsp;Vasilis J Promponas","doi":"10.1080/15548627.2023.2235851","DOIUrl":"10.1080/15548627.2023.2235851","url":null,"abstract":"<p><p>Several selective macroautophagy receptor and adaptor proteins bind members of the Atg8 (autophagy related 8) family using short linear motifs (SLiMs), most often referred to as Atg8-family interacting motifs (AIMs) or LC3-interacting regions (LIRs). AIM/LIR motifs have been extensively studied during the last fifteen years, since they can uncover the underlying biological mechanisms and possible substrates for this key catabolic process of eukaryotic cells. Prompted by the fact that experimental information regarding LIR motifs can be found scattered across heterogeneous literature resources, we have developed LIRcentral (https://lircentral.eu), a freely available online repository for user-friendly access to comprehensive, high-quality information regarding LIR motifs from manually curated publications. Herein, we describe the development of LIRcentral and showcase currently available data and features, along with our plans for the expansion of this resource. Information incorporated in LIRcentral is useful for accomplishing a variety of research tasks, including: (i) guiding wet biology researchers for the characterization of novel instances of LIR motifs, (ii) giving bioinformaticians/computational biologists access to high-quality LIR motifs for building novel prediction methods for LIR motifs and LIR containing proteins (LIRCPs) and (iii) performing analyses to better understand the biological importance/features of functional LIR motifs. We welcome feedback on the LIRcentral content and functionality by all interested researchers and anticipate this work to spearhead a community effort for sustaining this resource which will further promote progress in studying LIR motifs/LIRCPs.<b>Abbreviations</b>: AIM, Atg8-family interacting motif; Atg8, autophagy related 8; GABARAP, GABA type A receptor-associated protein; LIR, LC3-interacting region; LIRCP, LIR-containing protein; MAP1LC3/LC3, microtubule associated protein 1 light chain 3; PMID, PubMed identifier; PPI, protein-protein interaction; SLiM, short linear motif.</p>","PeriodicalId":8722,"journal":{"name":"Autophagy","volume":" ","pages":"3189-3200"},"PeriodicalIF":13.3,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10621281/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10296222","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
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