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杨树PagABP1介导生长素信号影响植株生长OA

PagABP1 in Populus Mediates Auxin Signaling to Influence Plant Growth

中文摘要英文摘要

[目的]对 84K杨PagABP基因家族进行全基因组鉴定和生物信息学分析,选择在顶芽、幼茎、形成层、韧皮部和木质部均高表达的PagABP1基因,探究该基因对杨树径向生长和高生长的调控作用,为阐明ABP1介导的生长素信号通路在茎生长中的分子机制提供参考.[方法]采用生物信息学相关方法,鉴定 84K杨PagABP基因家族成员;利用qRT-PCR技术,分析PagABP1基因在顶芽、幼叶、幼茎、幼根、成熟茎、老根、根尖、韧皮部、维管形成层和木质部中的表达;分别将PagABP1启动子和编码区序列构建植物PPagABP1::GUS启动子载体和过表达35S::PagABP1载体,应用农杆菌介导法创制 84K杨转基因材料,探究PagABP1基因对杨树径向生长和高生长的影响.[结果]在 84K杨基因组中鉴定到 2个ABP基因家族成员,其中PagABP1基因在顶芽、幼茎、形成层、韧皮部和木质部中相对表达量较高;PpagABP1::GUS转基因杨与PpagDR5::GUS(生长素响应报告基因)转基因杨基因表达位置重合,主要表达于顶芽、幼茎、形成层、韧皮部与初生木质部,提示PagABP1参与生长素诱导影响径向生长和高生长;截顶土栽苗在萌芽数和生长速率上,PagABP1-OE株系均显著大于对照;分析 60天的过表达PagABP1基因的转基因株系(#17、#26)发现,第 12茎节间形成层宽度、初生木质部宽度、韧皮部宽度、株高和地径分别较对照提高50.2%、43.3%、1.58%、19.14%和 19.29%.[结论]PagABP1基因与生长素表达部位关联,主要在顶芽、幼茎、形成层、韧皮部和初生木质部中表达,影响杨树径向生长和高生长.

[Objective]Through genome-wide identification and bioinformatics analysis of PagABP gene family of Populus alba×P.glandulosa,the gene PagABP1 that is highly expressed in young stems,cambium,xylem and phloem was selected to explore its effect on radial and height growth of this poplar.This study aims to provide a theoretical basis for elucidating how the auxin signaling pathway regulates secondary growth of stems by studying the regulatory role of this gene in the radial and height growth of poplars.[Method]Bioinformatics and related software were used to identify the members of the PagABP gene family in 84K poplar.The real-time fluorescence quantitative PCR was used to analyze the expression of PagABP1 gene in terminal buds,young leaves,young stems,young roots,mature stems,old roots,root tips,phloem,vascular cambium and xylem.Plant PPagABP1::GUS promoter vector and overexpressing 35S::PagABP1 vector were constructed by using the PagABP1 promoter and coding region sequences,respectively.Agrobacterium-mediated method was used to create 84K poplar transgenic materials that were used to identify the effects of PagABP1 gene on poplar radial and height growth.[Result]Two ABP homologous genes were identified in 84K poplar genome,and the PagABP1 gene showed relatively higher expression levels in the apical bud,young stems,phloem,cambium,and xylem.The expression locations of PPagABP1::GUS in transgenic poplar were overlapped with those of PpagDR5::GUS(auxin response reporter gene),mainly in the terminal bud,young stem,cambium,phloem,and primary xylem,suggesting that PagABP1 is involved in auxin-mediated regulation of radial and height growth.The germination number and growth rate of PagABP1-OE lines were significantly higher than those of the control when the truncated seedlings were planted in soil.Analysis of transgenic lines(#17、#26)that overexpressed PagABP1 gene at 60 days showed that the width of the cambium,primary xylem,and phloem of 12th internode,plant height and basal diameter increased by 50.2%,43.3%,1.58%,19.14%and 19.29%,respectively,compared to the control.[Conclusion]PagABP1 gene is associated with auxin expression site,mainly expressed in terminal buds,young stem,phloem,cambium,and primary xylem,affecting radial and height growth.This study can lay a foundation for further revealing the molecular mechanism of PagABP1 gene involved in stem growth of 84K poplar.

王深;舒文波;曾智新;乔静;王雨馨;郑瑞琦;王启;吴荟;张琦琦;焦阳

果蔬园艺作物种质创新与利用全国重点实验室 华中农业大学 武汉 430070||华中农业大学神农架科技创新中心 神农架 442422果蔬园艺作物种质创新与利用全国重点实验室 华中农业大学 武汉 430070||华中农业大学神农架科技创新中心 神农架 442422果蔬园艺作物种质创新与利用全国重点实验室 华中农业大学 武汉 430070||华中农业大学神农架科技创新中心 神农架 442422果蔬园艺作物种质创新与利用全国重点实验室 华中农业大学 武汉 430070||华中农业大学神农架科技创新中心 神农架 442422果蔬园艺作物种质创新与利用全国重点实验室 华中农业大学 武汉 430070果蔬园艺作物种质创新与利用全国重点实验室 华中农业大学 武汉 430070||华中农业大学神农架科技创新中心 神农架 442422果蔬园艺作物种质创新与利用全国重点实验室 华中农业大学 武汉 430070||华中农业大学神农架科技创新中心 神农架 442422果蔬园艺作物种质创新与利用全国重点实验室 华中农业大学 武汉 430070||华中农业大学神农架科技创新中心 神农架 442422果蔬园艺作物种质创新与利用全国重点实验室 华中农业大学 武汉 430070果蔬园艺作物种质创新与利用全国重点实验室 华中农业大学 武汉 430070||华中农业大学神农架科技创新中心 神农架 442422

农业科技

84K杨生长素信号PagABP1径向生长高生长

Populus alba×P.glandulosaauxin signalingPagABP1radial growthheight growth

《林业科学》 2026 (2)

126-133,8

国家重点研发计划项目(2023YFD2200202)湖北省大学生创新训练计划项目(S202410504140)华中农业大学2024年大学生科技创新基金(SRF)项目(2024SRF085).

10.11707/j.1001-7488.LYKX20250329

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