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毛花猕猴桃AeBAM基因家族鉴定及其表达分析OA

Identification and Expression Analysis of AeBAM Gene Family in Actinidia eriantha

中文摘要英文摘要

为解析毛花猕猴桃(Actinidia eriantha)β-淀粉酶(β-amylase,BAM)基因家族信息,基于毛花猕猴桃'赣绿 1 号'高质量参考基因组数据(PRJNA839193),鉴定了 AeBAM 家族成员并对其理化性质、进化关系进行了分析,同时利用转录组和 qRT-PCR 技术明确了 AeBAM 在不同组织及果实发育后期(淀粉降解期)的表达特征.在毛花猕猴桃中共鉴定出 17 个 AeBAM 成员,编码氨基酸数量在 189~751之间、理论等电点 5.24~10.01、分子量 21 149.85~84 142.08 Da.根据多物种进化树分析,BAM 可以分为 5 个亚族,其中 I 和 V 亚族成员居多;共线性分析表明,AeBAM 家族内部共存在 10 对复制基因对和5 对串联重复基因对,所有成员的 Ka/Ks比值均小于 1,在进化过程中受到纯化选择;AeBAM 家族基因启动子上含有大量的光响应、逆境胁迫和激素调控相关的顺式作用元件.转录组分析表明,AeBAM 成员表达具有组织特异性,其中 AeBAM5、AeBAM13 和 AeBAM16 在果实中具有较高的表达量且在果实套袋后表达量显著上升;qRT-PCR 表明,AeBAM5 和 AeBAM13 表达量在淀粉降解期显著上升并与淀粉降解负相关,可被认为是调控果实淀粉降解的关键基因家族成员.

To elucidate the characteristics of the β-amylase(BAM)gene family in Actinidia eriantha,AeBAM family members were identified based on high-quality reference genome of A.eriantha'Ganlü 1'(PRJNA839193),and their physicochemical properties and evolutionary relationships were analyzed.In addition,transcriptome sequencing and qRT-PCR analyses were performed to determine the expression profiles of AeBAM genes in different tissues and at the late fruit development(starch degradation stage).A total of seventeen AeBAM genes were identified in A.eriantha,encoding proteins ranging from 189 to 751 amino acids,with theoretical isoelectric points of 5.24-10.01 and molecular weights of 21 149.85-84 142.08 Da.Phylogenetic analysis across many species classified BAM into five subgroups,with subgroups I and V containing the majority members.Collinearity analysis revealed 10 pairs of duplicated gene pairs and 5 pairs of tandemly duplicated genes pairs within the family.All members showed Ka/Ks ratios less than 1,indicating they were purifying selection during evolution.Promoter analysis indicated that AeBAM genes contained numerous cis-acting elements related to light responsiveness,stress adaptation,and hormonal regulation.Transcriptome analysis showed that AeBAM genes exhibited tissue-specific expression patterns,among which AeBAM5,AeBAM13 and AeBAM16 were highly expressed in fruits,and their expression levels significant increased after bagging.qRT-PCR validation revealed that the expression levels of AeBAM5 and AeBAM13 increased significantly during the starch degradation stage and were negatively correlated with starch degradation,suggesting that they may be key members of the AeBAM gene family regulating fruit starch degradation.

陈钰珊;高欢;吴俊康;王莉梅;黄春辉;徐小彪;廖光联

江西农业大学农学院,南昌 330045||江西农业大学猕猴桃研究所,南昌 330045江西农业大学农学院,南昌 330045||江西农业大学猕猴桃研究所,南昌 330045江西农业大学农学院,南昌 330045||江西农业大学猕猴桃研究所,南昌 330045江西农业大学农学院,南昌 330045||江西农业大学猕猴桃研究所,南昌 330045江西农业大学农学院,南昌 330045||江西农业大学猕猴桃研究所,南昌 330045江西农业大学农学院,南昌 330045||江西农业大学猕猴桃研究所,南昌 330045江西农业大学农学院,南昌 330045||江西农业大学猕猴桃研究所,南昌 330045

农业科技

毛花猕猴桃β-淀粉酶淀粉表达分析

Actinidia erianthaβ-amylasestarchexpression analysis

《园艺学报》 2026 (3)

683-696,14

国家自然科学基金项目(32302490,32160692)

10.16420/j.issn.0513-353x.2025-0310

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