Plant Cell最新文献_第3页

ALTERED MERISTEM PROGRAM1 impairs RNA silencing by repressing the biogenesis of a subset of inverted repeat-derived siRNAs. ALTERED MERISTEM PROGRAM1 通过抑制反向重复衍生的 siRNAs 子集的生物生成来损害 RNA 沉默。

IF 1 1区生物学

Plant Cell Pub Date : 2024-12-23 DOI: 10.1093/plcell/koae293

Jing Li, Brandon Le, Xufeng Wang, Ye Xu, Suikang Wang, Hao Li, Lei Gao, Beixin Mo, Lin Liu, Xuemei Chen

{"title":"ALTERED MERISTEM PROGRAM1 impairs RNA silencing by repressing the biogenesis of a subset of inverted repeat-derived siRNAs.","authors":"Jing Li, Brandon Le, Xufeng Wang, Ye Xu, Suikang Wang, Hao Li, Lei Gao, Beixin Mo, Lin Liu, Xuemei Chen","doi":"10.1093/plcell/koae293","DOIUrl":"10.1093/plcell/koae293","url":null,"abstract":"RNA silencing negatively regulates gene expression at the transcriptional and posttranscriptional levels through DNA methylation, histone modification, mRNA cleavage, and translational inhibition. Small interfering RNAs (siRNAs) of 21 to 24 nucleotides are processed from double-stranded RNAs by Dicer-like (DCL) enzymes and play essential roles in RNA silencing in plants. Here, we demonstrated that ALTERED MERISTEM PROGRAM1 (AMP1) and its putative paralog LIKE AMP1 (LAMP1) impair RNA silencing by repressing the biogenesis of a subset of inverted repeat (IR)-derived siRNAs in Arabidopsis (Arabidopsis thaliana). AMP1 and LAMP1 inhibit Pol II-dependent IR gene transcription by suppressing ARGONAUTE 1 (AGO1) protein levels. Genetic analysis indicates that AMP1 acts upstream of RNA polymerase IV subunit 1 (NRPD1), RNA-dependent RNA polymerase 2 (RDR2), and DCL4, which are required for IR-induced RNA silencing. We also show that AMP1 and LAMP1 inhibit siRNA-mediated silencing in a different mechanism from that of AGO4 and DCL3. Together, these results reveal two previously unknown players in siRNA biogenesis from IRs-AGO1, which promotes IR transcription, and AMP1, which inhibits IR transcription indirectly through the repression of AGO1 expression.","PeriodicalId":20186,"journal":{"name":"Plant Cell","volume":" ","pages":""},"PeriodicalIF":10.0,"publicationDate":"2024-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11663600/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142576547","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

The transcription factors ERF105 and NAC72 regulate expression of a sugar transporter gene and hexose accumulation in grape. 转录因子ERF105和NAC72调控葡萄糖转运基因的表达和己糖的积累。

IF 1 1区生物学

Plant Cell Pub Date : 2024-12-23 DOI: 10.1093/plcell/koae326

Lizhen Lu, Serge Delrot, Peige Fan, Zhan Zhang, Die Wu, Fengqin Dong, Pedro García-Caparros, Shaohua Li, Zhanwu Dai, Zhenchang Liang

{"title":"The transcription factors ERF105 and NAC72 regulate expression of a sugar transporter gene and hexose accumulation in grape.","authors":"Lizhen Lu, Serge Delrot, Peige Fan, Zhan Zhang, Die Wu, Fengqin Dong, Pedro García-Caparros, Shaohua Li, Zhanwu Dai, Zhenchang Liang","doi":"10.1093/plcell/koae326","DOIUrl":"10.1093/plcell/koae326","url":null,"abstract":"Sugar transport plays a pivotal role in determining the productivity of plants and their capacity to act as carbon sinks. In the major fruit crop grapevine (Vitis vinifera L.), the transporter gene V. vinifera Sugars Will Eventually be Exported Transporter 15 (VvSWEET15) is strongly expressed during berry ripening. However, the specific functions of VvSWEET15 and the mechanisms governing its transcriptional regulation remain largely unresolved. Here, we demonstrate that VvSWEET15 functions as a hexose transporter whose expression is associated with the strong sugar accumulation that starts at the véraison stage. We also characterize VvERF105 as a repressor that binds to the LTR-binding element in the VvSWEET15 promoter, thereby downregulating its expression and inhibiting hexose accumulation at the prevéraison stage. In contrast, VvNAC72 is an activator that binds to the VvNAC72-binding domain (CACATG) and promotes VvSWEET15 expression and hexose accumulation at postvéraison stages. Both transcription factors and VvSWEET15 are preferentially expressed in phloem cells. These results demonstrate that the balance between transcriptional activators and repressors is critical in regulating VvSWEET15 expression in sink organs. Further understanding of these processes will help improve plant productivity and their potential to be used as carbon sinks.","PeriodicalId":20186,"journal":{"name":"Plant Cell","volume":" ","pages":""},"PeriodicalIF":10.0,"publicationDate":"2024-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142847475","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

Unraveled: The role of Arabidopsis GTE4-EML in transcription via two distinct histone modifications. 揭示：拟南芥GTE4-EML通过两种不同的组蛋白修饰在转录中的作用。

IF 1 1区生物学

Plant Cell Pub Date : 2024-12-23 DOI: 10.1093/plcell/koaf009

Pei Qin Ng

引用次数: 0

Feeling the heat: Long-term heat stress impairs growth but not photosynthesis in a C4 grass.

IF 1 1区生物学

Plant Cell Pub Date : 2024-12-23 DOI: 10.1093/plcell/koaf008

Guy Levin, Gadi Schuster

引用次数: 0

A natural variant of NON-RIPENING promotes fruit ripening in watermelon. NON-RIPENING 天然变体可促进西瓜果实成熟。

IF 1 1区生物学

Plant Cell Pub Date : 2024-12-23 DOI: 10.1093/plcell/koae313

Jinfang Wang, Yongtao Yu, Shaogui Guo, Jie Zhang, Yi Ren, Shouwei Tian, Maoying Li, Shengjin Liao, Guoyi Gong, Haiying Zhang, Yong Xu

{"title":"A natural variant of NON-RIPENING promotes fruit ripening in watermelon.","authors":"Jinfang Wang, Yongtao Yu, Shaogui Guo, Jie Zhang, Yi Ren, Shouwei Tian, Maoying Li, Shengjin Liao, Guoyi Gong, Haiying Zhang, Yong Xu","doi":"10.1093/plcell/koae313","DOIUrl":"10.1093/plcell/koae313","url":null,"abstract":"The regulation of non-climacteric fruit ripening by the transcription factor NON-RIPENING (NOR) is poorly understood. Here, we identified that the NOR homolog in the non-climacteric fruit watermelon (Citrullus lanatus) was located within the selective sweep and sweetness quantitative trait locus that was selected during domestication from landraces to cultivars. ClNOR knockout substantially delayed fruit ripening, and the fruits of the knockout plants had lower abscisic acid (ABA) levels, lighter colored flesh, and were less sweet compared to wild type. Transcriptome analysis and DNA affinity purification sequencing revealed that ClNOR targeted the Basic Leucine Zipper gene ClbZIP1, which links ClNOR to genes that do not have a ClNOR-binding motif in their promoters, such as the ABA biosynthesis gene, 9-cis-epoxycarotenoid dioxygenase ClNCED1 and the chromoplast phosphate transporter gene ClPHT4;2. The double mutant Clnor Clbzip1 exhibited delayed fruit ripening, lower ABA level, and lighter colored flesh. Its delayed ripening phenotype was stronger than that of the Clbzip1 single mutant. Additionally, the ClNORT,T haplotype in cultivated watermelon resulted in higher ClbZIP1 expression, but ClNORC,T from landraces and ClNORC,G from ancestral watermelon did not. Heterologous ClNORT,T expression rescued the delayed ripening phenotype of the Slnor knockout in tomato (Solanum lycopersicum). This natural variant (564T/C) of ClNOR promoted fruit ripening by enhancing target genes transcription. Overall, these findings will help elucidate the evolutionary mechanisms of nonclimacteric fruit ripening.","PeriodicalId":20186,"journal":{"name":"Plant Cell","volume":" ","pages":""},"PeriodicalIF":10.0,"publicationDate":"2024-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142740153","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 E3 ligase OsPUB33 controls rice grain size and weight by regulating the OsNAC120-BG1 module. E3连接酶OsPUB33通过调控OsNAC120-BG1模块来控制水稻谷粒的大小和重量。

IF 1 1区生物学

Plant Cell Pub Date : 2024-12-23 DOI: 10.1093/plcell/koae297

Zizhao Xie, Ying Sun, Chenghang Zhan, Chengfeng Qu, Ning Jin, Xinyue Gu, Junli Huang

{"title":"The E3 ligase OsPUB33 controls rice grain size and weight by regulating the OsNAC120-BG1 module.","authors":"Zizhao Xie, Ying Sun, Chenghang Zhan, Chengfeng Qu, Ning Jin, Xinyue Gu, Junli Huang","doi":"10.1093/plcell/koae297","DOIUrl":"10.1093/plcell/koae297","url":null,"abstract":"Grain size and weight are important determinants of crop yield. Although the ubiquitin pathway has been implicated in the grain development in rice (Oryza sativa), the underlying genetic and molecular mechanisms remain largely unknown. Here, we report that the plant U-box E3 ubiquitin ligase OsPUB33 interferes with the OsNAC120-BG1 module to control rice grain development. Functional loss of OsPUB33 triggers elevated photosynthetic rates and greater sugar translocation, leading to enhanced cell proliferation and accelerated grain filling. These changes cause enlarged spikelet hulls, thereby increasing final grain size and weight. OsPUB33 interacts with transcription factor OsNAC120, resulting in its ubiquitination and degradation. Unlike OsPUB33, OsNAC120 promotes grain size and weight: OsNAC120-overexpression plants harbor large and heavy grains, whereas osnac120 loss-of-function mutants produce small grains. Genetic interaction analysis supports that OsPUB33 and OsNAC120 function at least partially in a common pathway to control grain development, but have opposite functions. Additionally, OsNAC120 transcriptionally activates BIG GRAIN1 (BG1), a prominent modulator of grain size, whereas OsPUB33 impairs the OsNAC120-mediated regulation of BG1. Collectively, our findings uncover an important molecular framework for the control of grain size and weight by the OsPUB33-OsNAC120-BG1 regulatory module and provide promising targets for improving crop yield.","PeriodicalId":20186,"journal":{"name":"Plant Cell","volume":" ","pages":""},"PeriodicalIF":10.0,"publicationDate":"2024-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11663607/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142582983","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

Maternally expressed FERTILIZATION-INDEPENDENT ENDOSPERM1 regulates seed dormancy and aleurone development in rice. 母源表达的 OsFERTILIZATION INDEPENDENT ENDOSPERM1 调控水稻的种子休眠和胚乳发育。

IF 1 1区生物学

Plant Cell Pub Date : 2024-12-23 DOI: 10.1093/plcell/koae304

Xiaojun Cheng, Su Zhang, Zhiguo E, Zongju Yang, Sijia Cao, Rui Zhang, Baixiao Niu, Qian-Feng Li, Yong Zhou, Xin-Yuan Huang, Qiao-Quan Liu, Chen Chen

{"title":"Maternally expressed FERTILIZATION-INDEPENDENT ENDOSPERM1 regulates seed dormancy and aleurone development in rice.","authors":"Xiaojun Cheng, Su Zhang, Zhiguo E, Zongju Yang, Sijia Cao, Rui Zhang, Baixiao Niu, Qian-Feng Li, Yong Zhou, Xin-Yuan Huang, Qiao-Quan Liu, Chen Chen","doi":"10.1093/plcell/koae304","DOIUrl":"10.1093/plcell/koae304","url":null,"abstract":"Seed dormancy, an essential trait for plant adaptation, is determined by the embryo itself and the surrounding tissues. Here, we found that rice (Oryza sativa) FERTILIZATION-INDEPENDENT ENDOSPERM1 (OsFIE1) regulates endosperm-imposed dormancy and the dorsal aleurone thickness in a manner dependent on the parent of origin. Maternally expressed OsFIE1 suppresses gibberellin (GA) biosynthesis in the endosperm by depositing trimethylation of lysine 27 on histone H3 (H3K27me3) marks on GA biosynthesis-related genes, thus inhibiting germination and aleurone differentiation. Knockout of rice GA 20-oxidase1 (OsGA20ox1) alleviated the phenotypic defects in osfie1. The aleurone-positive determinant Crinkly 4 (OsCR4) is another target of the OsFIE1-containing Polycomb repressive complex 2 (PRC2). We found that OsFIE1 plays an important role in genomic imprinting in the endosperm of germinating seeds, particularly for paternally expressed genes associated with H3K27me3. The increased aleurone thickness of osfie1 substantially improved grain nutritional quality, indicating that the osfie1 gene may be utilized for breeding nutrient-enriched rice. The findings provide insights into the essential roles of PRC2-mediated H3K27me3 methylation in the acquisition of seed dormancy and endosperm cell differentiation in rice.","PeriodicalId":20186,"journal":{"name":"Plant Cell","volume":" ","pages":""},"PeriodicalIF":10.0,"publicationDate":"2024-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11663568/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142644315","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

Temperature-driven changes in membrane fluidity differentially impact FILAMENTATION TEMPERATURE-SENSITIVE H2-mediated photosystem II repair. 温度驱动的膜流动性变化对成丝温度敏感的h2介导的光系统II修复有不同的影响。

IF 1 1区生物学

Plant Cell Pub Date : 2024-12-23 DOI: 10.1093/plcell/koae323

Jingzhi Zhang, Keun Pyo Lee, Yanling Liu, Chanhong Kim

{"title":"Temperature-driven changes in membrane fluidity differentially impact FILAMENTATION TEMPERATURE-SENSITIVE H2-mediated photosystem II repair.","authors":"Jingzhi Zhang, Keun Pyo Lee, Yanling Liu, Chanhong Kim","doi":"10.1093/plcell/koae323","DOIUrl":"10.1093/plcell/koae323","url":null,"abstract":"The Arabidopsis (Arabidopsis thaliana) yellow variegated2 (var2) mutant, lacking functional FILAMENTATION TEMPERATURE-SENSITIVE H2 (FtsH2), an ATP-dependent zinc metalloprotease, is a powerful tool for studying the photosystem II (PSII) repair process in plants. FtsH2, forming hetero-hexamers with FtsH1, FtsH5, and FtsH8, plays an indispensable role in PSII proteostasis. Although abiotic stresses like cold and heat increase chloroplast reactive oxygen species (ROS) and PSII damage, var2 mutants behave like wild-type plants under heat stress but collapse under cold stress. Our study on transgenic var2 lines expressing FtsH2 variants, defective in either substrate extraction or proteolysis, reveals that cold stress causes an increase in membrane viscosity, demanding more substrate extraction power than proteolysis by FtsH2. Overexpression of FtsH2 lacking substrate extraction activity does not rescue the cold-sensitive phenotype, while overexpression of FtsH2 lacking protease activity does in var2, with other FtsH isomers present. This indicates that FtsH2's substrate extraction activity is indispensable under cold stress when membranes become more viscous. As temperatures rise and membrane fluidity increases, substrate extraction activity from other isomers suffices, explaining the var2 mutant's heat stress resilience. These findings underscore the direct effect of membrane fluidity on the functionality of the thylakoid FtsH complex under stress. Future research should explore how membrane fluidity impacts proteostasis, potentially uncovering strategies to modulate thermosensitivity.","PeriodicalId":20186,"journal":{"name":"Plant Cell","volume":" ","pages":""},"PeriodicalIF":10.0,"publicationDate":"2024-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11684078/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142813461","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

XYLAN O-ACETYLTRANSFERASE 6 promotes xylan synthesis by forming a complex with IRX10 and governs wall formation in rice. 木聚糖o -乙酰转移酶6通过与IRX10形成复合物促进木聚糖合成，并控制水稻细胞壁的形成。

IF 1 1区生物学

Plant Cell Pub Date : 2024-12-23 DOI: 10.1093/plcell/koae322

Zhao Wen, Zuopeng Xu, Lanjun Zhang, Yi Xue, Hang Wang, Lin Jian, Jianing Ma, Zhuolin Liu, Hanlei Yang, Shaohui Huang, Xue Kang, Yihua Zhou, Baocai Zhang

{"title":"XYLAN O-ACETYLTRANSFERASE 6 promotes xylan synthesis by forming a complex with IRX10 and governs wall formation in rice.","authors":"Zhao Wen, Zuopeng Xu, Lanjun Zhang, Yi Xue, Hang Wang, Lin Jian, Jianing Ma, Zhuolin Liu, Hanlei Yang, Shaohui Huang, Xue Kang, Yihua Zhou, Baocai Zhang","doi":"10.1093/plcell/koae322","DOIUrl":"10.1093/plcell/koae322","url":null,"abstract":"Xylan, a pivotal polymer with diversified structures, is indispensable for cell wall integrity and contributes to plant growth and biomass recalcitrance. Xylan is synthesized by multienzyme complexes named xylan synthase complexes (XSCs). However, the biochemical mechanism of XSCs and the functions of core components within XSC remain unclear. Here, we report that rice (Oryza sativa) XYLAN O-ACETYLTRANSFERASE 6 (XOAT6) and the xylan synthase IRREGULAR XYLEM10 (IRX10) represent core components of the XSC, acting together to biosynthesize acetyl-xylans. Co-fractionation mass spectrometry and protein-protein interaction analyses revealed that IRX10 and XOAT6 physically interact within XSC, corroborated by similar xylan defects in xoat6 and irx10 mutants. Biochemical assays showed that XOAT6 is an O-acetyltransferase of the xylan backbone and facilitates chain polymerization catalyzed by IRX10. Fluorescence correlation spectroscopy further visualized the xylooligomer polymerization process at a single-molecule level. Solid-state NMR analysis, electron microscopy observations, and nanoindentation examinations identified the altered xylan conformation, disorganized cellulosic structure, and increased wall rigidity and cellulose accessibility in the mutants, leading to brittleness and improved saccharification efficiency. Our findings provide insights into the assembly of XSCs and xylan biosynthesis and offer a framework for tailoring xylans to improve crop traits and biomass.","PeriodicalId":20186,"journal":{"name":"Plant Cell","volume":" ","pages":""},"PeriodicalIF":10.0,"publicationDate":"2024-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11684075/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142813787","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

Jasmonate induces translation of the Arabidopsis transfer RNA-binding protein YUELAO1, which activates MYC2 in jasmonate signaling. 茉莉酸诱导拟南芥 tRNA 结合蛋白 YUELAO1 翻译，从而激活茉莉酸信号转导中的 MYC2。

IF 1 1区生物学

Plant Cell Pub Date : 2024-12-23 DOI: 10.1093/plcell/koae294

Jiahui Wang, Yuanyuan Li, Yanru Hu, Sirui Zhu

{"title":"Jasmonate induces translation of the Arabidopsis transfer RNA-binding protein YUELAO1, which activates MYC2 in jasmonate signaling.","authors":"Jiahui Wang, Yuanyuan Li, Yanru Hu, Sirui Zhu","doi":"10.1093/plcell/koae294","DOIUrl":"10.1093/plcell/koae294","url":null,"abstract":"Jasmonate is ubiquitous in the plant kingdom and regulates multiple physiological processes. Although jasmonate signaling has been thoroughly investigated in Arabidopsis thaliana, most studies have focused on the transcriptional mechanisms underlying various jasmonate responses. It remains unclear whether (and how) translation-related pathways help improve transcription efficiency to modulate jasmonate signaling, which may enable plants to respond to stressful conditions effectively. Here, we demonstrate that jasmonate induces translation of the transfer RNA (tRNA)-binding protein YUELAO 1 (YL1) via a specific region in its 3' untranslated region (3' UTR). YL1 and its homolog YL2 redundantly stimulate jasmonate responses such as anthocyanin accumulation and root growth inhibition, with the YL1 3' UTR being critical for YL1-promoted jasmonate responses. Once translated, YL1 acts as an activator of the MYC2 transcription factor through direct interaction, and disrupting YL1 3' UTR impairs the YL1-mediated transcriptional activation of MYC2. YL1 enhances jasmonate responses mainly in a MYC2-dependent manner. Together, these findings reveal a translational mechanism involved in jasmonate signaling and advance our understanding of the transcriptional regulation of jasmonate signaling. The YL1 3' UTR acts as a crucial signal transducer that integrates translational and transcriptional regulation, allowing plants to respond to jasmonate in a timely fashion.","PeriodicalId":20186,"journal":{"name":"Plant Cell","volume":" ","pages":""},"PeriodicalIF":10.0,"publicationDate":"2024-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11663558/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142569413","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