{"title":"Upstairs, Downstairs - conserved and divergent CLAVATA signalling in shoot meristem development and root symbioses.","authors":"Tiana Scott, Alejandro Correa-Lozano, Eloise Foo","doi":"10.1093/aob/mcae192","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>The CLV3/EMBRYO-SURROUNDING REGION (CLE) peptides control plant development and response to the environment. Key conserved roles include the regulation of shoot apical meristems and the long-distance control of root colonisation by nutrient-acquiring microbes, including the widespread symbioses with arbuscular mycorrhizal fungi and nodulation with nitrogen-fixing bacteria in legumes. At least some signalling elements appear to operate across both processes but clear gaps in our understanding remain. In legumes, although CLE peptide signalling has been examined in detail in symbioses, the role of this pathway in SAM development of legumes is poorly understood.</p><p><strong>Scope: </strong>In this Research in Context, we review the literature to clarify the conserved and divergent elements of the CLAVATA-CLE peptide signalling pathways that control SAM, mycorrhizal colonisation and nodulation. We used novel pea mutants to determine the role of CLE signalling in regulating SAM development of a model legume, including interaction with temperature.</p><p><strong>Conclusions: </strong>We found that in pea both genetic and environmental buffering of the CLE pathway influences SAM development. In pea, the CLAVATA2 (CLV2) CLE receptor-like protein and the unknown gene product encoded by the K301 gene are required to limit SAM size and floral organ production under cool temperatures. In contrast, the CLAVATA1 receptor-like kinase promotes SAM proliferation and appears to do so via a CLV2-independent pathway. In contrast, we found no role for the RDN1 enzyme, capable of arabinosylating CLE peptides, in SAM development. Future studies in other legumes are required to examine the role of other CLE peptide signalling elements in SAM control. Studies in non-vascular mycorrhizal hosts could explore if symbioses control is also an ancestral role for this signalling pathway.</p>","PeriodicalId":8023,"journal":{"name":"Annals of botany","volume":null,"pages":null},"PeriodicalIF":3.6000,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of botany","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/aob/mcae192","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Background: The CLV3/EMBRYO-SURROUNDING REGION (CLE) peptides control plant development and response to the environment. Key conserved roles include the regulation of shoot apical meristems and the long-distance control of root colonisation by nutrient-acquiring microbes, including the widespread symbioses with arbuscular mycorrhizal fungi and nodulation with nitrogen-fixing bacteria in legumes. At least some signalling elements appear to operate across both processes but clear gaps in our understanding remain. In legumes, although CLE peptide signalling has been examined in detail in symbioses, the role of this pathway in SAM development of legumes is poorly understood.
Scope: In this Research in Context, we review the literature to clarify the conserved and divergent elements of the CLAVATA-CLE peptide signalling pathways that control SAM, mycorrhizal colonisation and nodulation. We used novel pea mutants to determine the role of CLE signalling in regulating SAM development of a model legume, including interaction with temperature.
Conclusions: We found that in pea both genetic and environmental buffering of the CLE pathway influences SAM development. In pea, the CLAVATA2 (CLV2) CLE receptor-like protein and the unknown gene product encoded by the K301 gene are required to limit SAM size and floral organ production under cool temperatures. In contrast, the CLAVATA1 receptor-like kinase promotes SAM proliferation and appears to do so via a CLV2-independent pathway. In contrast, we found no role for the RDN1 enzyme, capable of arabinosylating CLE peptides, in SAM development. Future studies in other legumes are required to examine the role of other CLE peptide signalling elements in SAM control. Studies in non-vascular mycorrhizal hosts could explore if symbioses control is also an ancestral role for this signalling pathway.
背景:CLV3/EMBRYO-SURROUNDING REGION(CLE)肽控制植物的发育和对环境的反应。主要的保守作用包括调节嫩枝顶端分生组织和远距离控制营养获取微生物的根定植,包括豆科植物中广泛存在的与丛枝菌根真菌的共生以及与固氮菌的结瘤。至少有一些信号元素似乎在这两个过程中都起作用,但我们的认识仍然存在明显差距。在豆科植物中,虽然 CLE 肽信号在共生中得到了详细研究,但这一途径在豆科植物 SAM 发育中的作用却鲜为人知:在这篇 "背景研究"(Research in Context)中,我们回顾了相关文献,以阐明控制 SAM、菌根定殖和结瘤的 CLAVATA-CLE 肽信号通路中的保守和分歧因素。我们利用新型豌豆突变体来确定 CLE 信号在调控模式豆科植物 SAM 发育中的作用,包括与温度的相互作用:我们发现,在豌豆中,CLE 通路的遗传和环境缓冲都会影响 SAM 的发育。在豌豆中,CLAVATA2(CLV2)CLE 受体样蛋白和 K301 基因编码的未知基因产物是在低温条件下限制 SAM 大小和花器官生成所必需的。相反,CLAVATA1 受体样激酶能促进 SAM 的增殖,而且似乎是通过一种不依赖于 CLV2 的途径实现的。与此相反,我们没有发现 RDN1 酶在 SAM 发育中的作用,该酶能对 CLE 肽进行阿拉伯糖基化。未来需要对其他豆科植物进行研究,以考察其他 CLE 肽信号元件在 SAM 控制中的作用。对非维管束菌根宿主的研究可以探索共生控制是否也是该信号途径的一个祖先角色。
期刊介绍:
Annals of Botany is an international plant science journal publishing novel and rigorous research in all areas of plant science. It is published monthly in both electronic and printed forms with at least two extra issues each year that focus on a particular theme in plant biology. The Journal is managed by the Annals of Botany Company, a not-for-profit educational charity established to promote plant science worldwide.
The Journal publishes original research papers, invited and submitted review articles, ''Research in Context'' expanding on original work, ''Botanical Briefings'' as short overviews of important topics, and ''Viewpoints'' giving opinions. All papers in each issue are summarized briefly in Content Snapshots , there are topical news items in the Plant Cuttings section and Book Reviews . A rigorous review process ensures that readers are exposed to genuine and novel advances across a wide spectrum of botanical knowledge. All papers aim to advance knowledge and make a difference to our understanding of plant science.