Plant and Cell Physiology最新文献_第9页

Plant and Cell Physiology Reviewer Acknowledgments for 2023. 2023年植物与细胞生理学审稿人致谢

IF 3.9 2区生物学

Plant and Cell Physiology Pub Date : 2024-12-09 DOI: 10.1093/pcp/pcae139

引用次数: 0

Light-chilling Stress Causes Hyper-accumulation of Iron in Shoot, Exacerbating Leaf Oxidative Damage in Cucumber. 光冷胁迫会导致黄瓜嫩芽中铁的过度积累，加剧叶片的氧化损伤。

IF 3.9 2区生物学

Plant and Cell Physiology Pub Date : 2024-12-06 DOI: 10.1093/pcp/pcae111

Ko Takeuchi, Kumiko Ochiai, Masaru Kobayashi, Kouichi Kuroda, Kentaro Ifuku

{"title":"Light-chilling Stress Causes Hyper-accumulation of Iron in Shoot, Exacerbating Leaf Oxidative Damage in Cucumber.","authors":"Ko Takeuchi, Kumiko Ochiai, Masaru Kobayashi, Kouichi Kuroda, Kentaro Ifuku","doi":"10.1093/pcp/pcae111","DOIUrl":"10.1093/pcp/pcae111","url":null,"abstract":"Iron availability within the root system of plants fluctuates depending on various soil factors, which directly impacts plant growth. Simultaneously, various environmental stressors, such as high/low temperatures and high light intensity, affect plant photosynthesis in the leaves. However, the combined effects of iron nutrient conditions and abiotic stresses have not yet been clarified. In this study, we analyzed how iron nutrition conditions impact the chilling-induced damage on cucumber leaves (Cucumis sativus L.). When cucumbers were grown under different iron conditions and then exposed to chilling stress, plants grown under a high iron condition exhibited more severe chilling-induced damage than the control plants. Conversely, plants grown under a low-iron condition showed an alleviation of the chilling-induced damages. These differences were observed in a light-dependent manner, indicating that iron intensified the toxicity of reactive oxygen species generated by photosynthetic electron transport. In fact, plants grown under the low-iron condition showed less accumulation of malondialdehyde derived from lipid peroxidation after chilling stress. Notably, the plants grown under the high iron condition displayed a significant accumulation of iron and an increase in lipid peroxidation in the shoot, specifically after light-chilling stress, but not after dark-chilling stress. This indicated that increased root-to-shoot iron translocation, driven by light and low temperature, exacerbated leaf oxidative damage during chilling stress. These findings also highlight the importance of managing iron nutrition in the face of chilling stress and will facilitate crop breeding and cultivation strategies.","PeriodicalId":20575,"journal":{"name":"Plant and Cell Physiology","volume":" ","pages":"1873-1887"},"PeriodicalIF":3.9,"publicationDate":"2024-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142352646","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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 Armor of Orchid Petals: Insights into Cuticle Deposition Regulation. 兰花花瓣的盔甲：洞察角质层沉积调节

IF 3.9 2区生物学

Plant and Cell Physiology Pub Date : 2024-12-06 DOI: 10.1093/pcp/pcae116

Xiujuan Yang

引用次数: 0

FINE CULM1 Encoding a TEOSINTE BRANCHED1-like TCP Transcription Factor Negatively Regulates Axillary Meristem Formation in Rice. 编码 TEOSINTE BRANCHED1-like TCP 转录因子的 FINE CULM1 负向调控水稻腋生分生组织的形成。

IF 3.9 2区生物学

Plant and Cell Physiology Pub Date : 2024-12-06 DOI: 10.1093/pcp/pcae109

Wakana Tanaka, Ami Ohyama, Taiyo Toriba, Rumi Tominaga, Hiro-Yuki Hirano

{"title":"FINE CULM1 Encoding a TEOSINTE BRANCHED1-like TCP Transcription Factor Negatively Regulates Axillary Meristem Formation in Rice.","authors":"Wakana Tanaka, Ami Ohyama, Taiyo Toriba, Rumi Tominaga, Hiro-Yuki Hirano","doi":"10.1093/pcp/pcae109","DOIUrl":"10.1093/pcp/pcae109","url":null,"abstract":"Shoot branching is a critical determinant of plant architecture and a key factor affecting crop yield. The shoot branching involves two main processes: axillary meristem formation and subsequent bud outgrowth. While considerable progress has been made in elucidating the genetic mechanisms underlying the latter process, our understanding of the former process remains limited. Rice FINE CULM1 (FC1), which is an ortholog of teosinte branched1 in maize (Zea mays) and BRANCHED1/2 in Arabidopsis (Arabidopsis thaliana), is known to act in the latter process by repressing bud outgrowth. In this study, we found that FC1 also plays a role in the former process, i.e. axillary meristem formation, in rice. This study was triggered by our unexpected observation that fc1 mutation suppresses the loss of axillary meristems in the loss-of-function mutant of the rice WUSCHEL gene TILLERS ABSENT1 (TAB1). In tab1 fc1, unlike in tab1, both stem cells and undifferentiated cells were maintained during axillary meristem formation, similar to the wild type. Morphological analysis showed that axillary meristem formation was accelerated in fc1, compared to the wild type. Consistent with this, cell proliferation was more active in the region containing stem cells and undifferentiated cells during axillary meristem formation in fc1 than in the wild type. Taken altogether, these findings suggest that FC1 negatively regulates axillary meristem formation by mildly repressing cell proliferation during this process.","PeriodicalId":20575,"journal":{"name":"Plant and Cell Physiology","volume":" ","pages":"1862-1872"},"PeriodicalIF":3.9,"publicationDate":"2024-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142473129","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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

Heritable Tissue-Culture-Free Gene Editing in Nicotiana benthamiana through Viral Delivery of SpCas9 and sgRNA. 通过病毒递送 SpCas9 和 sgRNA 在烟草中进行可遗传的无组织培养基因编辑。

IF 3.9 2区生物学

Plant and Cell Physiology Pub Date : 2024-12-06 DOI: 10.1093/pcp/pcae100

Tetsuya Yoshida, Masayuki Ishikawa, Seiichi Toki, Kazuhiro Ishibashi

{"title":"Heritable Tissue-Culture-Free Gene Editing in Nicotiana benthamiana through Viral Delivery of SpCas9 and sgRNA.","authors":"Tetsuya Yoshida, Masayuki Ishikawa, Seiichi Toki, Kazuhiro Ishibashi","doi":"10.1093/pcp/pcae100","DOIUrl":"10.1093/pcp/pcae100","url":null,"abstract":"Conventional plant gene editing requires laborious tissue-culture-mediated transformation, which restricts the range of applicable plant species. In this study, we developed a heritable and tissue-culture-free gene editing method in Nicotiana benthamiana using tobacco ringspot virus (TRSV) as a vector for in planta delivery of Cas9 and single-guide RNA (sgRNA) to shoot apical meristems. Agrobacterium-mediated inoculation of the TRSV vector induced systemic and heritable gene editing in Nicotiana benthamiana PHYTOENE DESATURASE. Transient downregulation of RNA silencing enhanced gene editing efficiency, resulting in an order of magnitude increase (0.8-13.2%) in the frequency of transgenerational gene editing. While the TRSV system had a preference for certain sgRNA sequences, co-inoculation of a TRSV vector carrying only Cas9 and a tobacco rattle virus vector carrying sgRNA successfully introduced systemic mutations with all five tested sgRNAs. Extensively gene-edited lateral shoots occasionally grew from plants inoculated with the virus vectors, the transgenerational gene editing frequency of which ranged up to 100%. This virus-mediated heritable gene editing method makes plant gene editing easy, requiring only the inoculation of non-transgenic plants with a virus vector(s) to obtain gene-edited individuals.","PeriodicalId":20575,"journal":{"name":"Plant and Cell Physiology","volume":" ","pages":"1743-1750"},"PeriodicalIF":3.9,"publicationDate":"2024-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11631083/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142111314","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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

A Kinesin-Like Protein, KAC, is Required for Light-Induced and Actin-Based Chloroplast Movement in Marchantia polymorpha. 一种驱动蛋白样蛋白 KAC 是光诱导和基于肌动蛋白的叶绿体运动所必需的。

IF 3.9 2区生物学

Plant and Cell Physiology Pub Date : 2024-12-06 DOI: 10.1093/pcp/pcae101

Yoshiko Yamamoto-Negi, Takeshi Higa, Aino Komatsu, Kanta Sasaki, Kimitsune Ishizaki, Ryuichi Nishihama, Eiji Gotoh, Takayuki Kohchi, Noriyuki Suetsugu

{"title":"A Kinesin-Like Protein, KAC, is Required for Light-Induced and Actin-Based Chloroplast Movement in Marchantia polymorpha.","authors":"Yoshiko Yamamoto-Negi, Takeshi Higa, Aino Komatsu, Kanta Sasaki, Kimitsune Ishizaki, Ryuichi Nishihama, Eiji Gotoh, Takayuki Kohchi, Noriyuki Suetsugu","doi":"10.1093/pcp/pcae101","DOIUrl":"10.1093/pcp/pcae101","url":null,"abstract":"Chloroplasts accumulate on the cell surface under weak light conditions to efficiently capture light but avoid strong light to minimize photodamage. The blue light receptor phototropin regulates the chloroplast movement in various plant species. In Arabidopsis thaliana, phototropin mediates the light-induced chloroplast movement and positioning via specialized actin filaments on the chloroplasts, chloroplast-actin filaments. KINESIN-LIKE PROTEIN FOR ACTIN-BASED CHLOROPLAST MOVEMENT (KAC) and CHLOROPLAST UNUSUAL POSITIONING 1 (CHUP1) are pivotal for actin-based chloroplast movement and positioning in land plants. However, the mechanisms by which KAC and CHUP1 regulate chloroplast movement and positioning remain unclear. In this study, we characterized KAC and CHUP1 orthologs in the liverwort Marchantia polymorpha, MpKAC and MpCHUP1, respectively. Their knockout mutants, Mpkacko and Mpchup1ko, impaired the light-induced chloroplast movement. Although Mpchup1ko showed mild chloroplast aggregation, Mpkacko displayed severe chloroplast aggregation, suggesting the greater contribution of MpKAC to the chloroplast anchorage to the plasma membrane. Analysis of the subcellular localization of the functional MpKAC-Citrine indicated that MpKAC-Citrine formed a punctate structure on the plasma membrane. Structure-function analysis of MpKAC revealed that the deletion of the conserved C-terminal domain abrogates its targeting to the plasma membrane and its function. The deletion of the N-terminal motor domain retains the plasma membrane targeting but abrogates the formation of punctate structure and shows a severe defect in the light-induced chloroplast movement. Our findings suggest that the formation of the punctate structure on the plasma membrane of MpKAC is essential for chloroplast movement.","PeriodicalId":20575,"journal":{"name":"Plant and Cell Physiology","volume":" ","pages":"1787-1800"},"PeriodicalIF":3.9,"publicationDate":"2024-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142111312","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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

Minimized Dark Consumption of Calvin Cycle Intermediates Facilitates the Initiation of Photosynthesis in Synechocystis sp. PCC 6803. 将卡尔文循环中间产物的暗消耗减至最低可促进 Synechocystis sp. PCC 6803 开始光合作用。

IF 3.9 2区生物学

Plant and Cell Physiology Pub Date : 2024-12-06 DOI: 10.1093/pcp/pcae102

Kenya Tanaka, Akihiko Kondo, Tomohisa Hasunuma

{"title":"Minimized Dark Consumption of Calvin Cycle Intermediates Facilitates the Initiation of Photosynthesis in Synechocystis sp. PCC 6803.","authors":"Kenya Tanaka, Akihiko Kondo, Tomohisa Hasunuma","doi":"10.1093/pcp/pcae102","DOIUrl":"10.1093/pcp/pcae102","url":null,"abstract":"Cyanobacteria intricately regulate their metabolic pathways during the diurnal cycle to ensure survival and growth. Under dark conditions, the breakdown of glycogen, an energy reserve, in these organisms replenishes Calvin cycle intermediates, especially downstream glycolytic metabolites, which are necessary for photosynthesis initiation upon light irradiation. However, it remains unclear how the accumulation of these intermediates is maintained in the dark despite limited glycogen availability. Therefore, in this study, we investigated the regulation of downstream glycolytic metabolites of the Calvin cycle under dark and light conditions using Synechocystis sp. PCC 6803. Our results showed that during the dark period, low pyruvate kinase (Pyk) activity ensured metabolite accumulation, while endogenous Pyk overexpression significantly lowered the accumulation of glycolytic intermediates. Remarkably, wild-type Synechocystis maintained oxygen evolution ability throughout dark treatment for over 2 d, while Pyk overexpression resulted in decreased oxygen evolution after 16 h of dark treatment. These results indicated that limiting Pyk activity via darkness treatment facilitates photosynthetic initiation by maintaining glycolytic intermediates. Similarly, phosphoenolpyruvate carboxylase (PepC) overexpression decreased oxygen evolution under dark treatment; however, its effect was lower than that of Pyk. Furthermore, we noted that as PepC overexpression decreased the levels of glycolytic intermediates in the dark, sugar phosphates in the Calvin-Benson-Bassham (CBB) cycle showed high accumulation, suggesting that sugar phosphates play important roles in supporting photosynthesis initiation. Therefore, our study highlights the importance of controlling the metabolic pathways through which glycolytic and CBB cycle intermediates are consumed (defined as cataplerosis of the CBB cycle) to ensure stable photosynthesis.","PeriodicalId":20575,"journal":{"name":"Plant and Cell Physiology","volume":" ","pages":"1812-1820"},"PeriodicalIF":3.9,"publicationDate":"2024-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142140881","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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

Correction To: Auxin Biosynthesis, Accumulation, Action and Transport are Involved in Stress-Induced Microspore Embryogenesis Initiation and Progression in Brassica Napus. 修正：生长素的合成、积累、作用和运输参与了胁迫诱导的甘蓝型油菜小孢子胚胎发生、发生和发展。

IF 3.9 2区生物学

Plant and Cell Physiology Pub Date : 2024-12-06 DOI: 10.1093/pcp/pcae125

引用次数: 0

The HD-ZIP II Gene PaHAT14 Increases Cuticle Deposition by Downregulating ERF Gene PaERF105 in Phalaenopsis. HD-ZIP II 基因 PaHAT14 通过下调蝴蝶兰中的 ERF 基因 PaERF105 来增加角质层的沉积。

IF 3.9 2区生物学

Plant and Cell Physiology Pub Date : 2024-12-06 DOI: 10.1093/pcp/pcae078

Wan-Ting Mao, Wei-Han Hsu, Jia-Lin Song, Chang-Hsien Yang

{"title":"The HD-ZIP II Gene PaHAT14 Increases Cuticle Deposition by Downregulating ERF Gene PaERF105 in Phalaenopsis.","authors":"Wan-Ting Mao, Wei-Han Hsu, Jia-Lin Song, Chang-Hsien Yang","doi":"10.1093/pcp/pcae078","DOIUrl":"10.1093/pcp/pcae078","url":null,"abstract":"To analyze the genes involved in orchid floral development, a homeodomain-leucine zipper II gene PaHAT14, which is specifically and highly expressed in perianth during early flower development, was identified from Phalaenopsis. Transgenic Arabidopsis plants expressing 35S::PaHAT14 and 35S::PaHAT14 + SRDX (fused with the repressor motif SRDX) exhibited similar altered phenotypes, including small leaves, early flowering and bending petals with increased cuticle production. This suggests that PaHAT14 acts as a repressor. In contrast, transgenic Arabidopsis plants expressing 35S::PaHAT14 + VP16 (fused with the activation domain VP16) exhibited curled leaves, late flowering and folded petals with decreased cuticle production within hardly opened flowers. Additionally, the expression of the ERF gene DEWAX2, which negatively regulates cuticular wax biosynthesis, was downregulated in 35S::PaHAT14 and 35S::PaHAT14 + SRDX transgenic Arabidopsis, while it was upregulated in 35S::PaHAT14 + VP16 transgenic Arabidopsis. Furthermore, transient overexpression of PaHAT14 in Phalaenopsis petal/sepal increased cuticle deposition due to the downregulation of PaERF105, a Phalaenopsis DEWAX2 ortholog. On the other hand, transient overexpression of PaERF105 decreased cuticle deposition, whereas cuticle deposition increased and the rate of epidermal water loss was reduced in PaERF105 virus-induced gene silencing Phalaenopsis flowers. Moreover, ectopic expression of PaERF105 not only produced phenotypes similar to those in 35S::PaHAT14 + VP16 Arabidopsis but also compensated for the altered phenotypes observed in 35S::PaHAT14 and 35S::PaHAT14 + SRDX Arabidopsis. These results suggest that PaHAT14 promotes cuticle deposition by negatively regulating downstream gene PaERF105 in orchid flowers.","PeriodicalId":20575,"journal":{"name":"Plant and Cell Physiology","volume":" ","pages":"1751-1768"},"PeriodicalIF":3.9,"publicationDate":"2024-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141580666","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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

Arabidopsis Pentatricopeptide Repeat Protein GEND2 Participates in Mitochondrial RNA Editing. 拟南芥五肽重复蛋白 GEND2 参与线粒体 RNA 编辑。

IF 3.9 2区生物学

Plant and Cell Physiology Pub Date : 2024-12-06 DOI: 10.1093/pcp/pcae108

Yaqing Nie, Yan Li, Penglai Yuan, Chengyun Wu, Xiaoqing Wang, Chunfei Wang, Xiumei Xu, Zhenguo Shen, Zhubing Hu

{"title":"Arabidopsis Pentatricopeptide Repeat Protein GEND2 Participates in Mitochondrial RNA Editing.","authors":"Yaqing Nie, Yan Li, Penglai Yuan, Chengyun Wu, Xiaoqing Wang, Chunfei Wang, Xiumei Xu, Zhenguo Shen, Zhubing Hu","doi":"10.1093/pcp/pcae108","DOIUrl":"10.1093/pcp/pcae108","url":null,"abstract":"In Arabidopsis, RNA editing alters more than 500 cytidines (C) to uridines (U) in mitochondrial transcripts, a process involving the family of pentatricopeptide repeat (PPR) proteins. Here, we report a previously uncharacterized mitochondrial PLS-type PPR protein, GEND2, which functions in the mitochondrial RNA editing. The T-DNA insertion in the 5'-untranslated region of GEND2, referred to as gend2-1, results in defective root development compared to wild-type (WT) plants. A comprehensive examination of mitochondrial RNA-editing sites revealed a significant reduction in the gend2-1 mutant compared to WT plants, affecting six specific mitochondrial RNA editing sites, notably within the mitochondrial genes CcmFn-1, RPSL2 and ORFX. These genes encode critical components of cytochrome protein maturation pathway, mitochondrial ribosomal subunit and twin arginine translocation subunits, respectively. Further analysis of the transcriptional profile of the gend2-1 mutant and WT revealed a striking induction of expression in a cluster of genes associated with mitochondrial dysfunction and regulated by ANAC017, a key regulator coordinating organelle functions and stress responses. Intriguingly, the gend2-1 mutation activated an ANAC017-dependent signaling aimed at countering cell wall damage induced by cellulose synthase inhibitors, as well as an ANAC017-independent pathway that retarded root growth under normal condition. Collectively, our findings identify a novel mitochondrial PLS-type PPR protein GEND2, which participates in the editing of six specific mitochondrial RNA editing sites. Furthermore, the gend2-1 mutation triggers two distinct pathways in plants: an ANAC017-dependent pathway and ANAC017-independent pathway.","PeriodicalId":20575,"journal":{"name":"Plant and Cell Physiology","volume":" ","pages":"1849-1861"},"PeriodicalIF":3.9,"publicationDate":"2024-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142293933","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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