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园艺学报 ›› 2022, Vol. 49 ›› Issue (2): 341-351.doi: 10.16420/j.issn.0513-353x.2020-1041

• 研究论文 • 上一篇    下一篇

甜瓜果柄离区细胞学观察及成熟脱落基因AL3的初步定位

盛云燕1, 杨丽敏1, 戴冬洋1, 张佳欣1, 王岭1, 王迪2, 才羿1, 田丽美1,*()   

  1. 1黑龙江八一农垦大学园艺园林学院,黑龙江大庆 163319
    2黑龙江省农业科学院大庆分院,黑龙江大庆 163310
  • 收稿日期:2021-05-11 修回日期:2021-11-03 出版日期:2022-02-25 发布日期:2022-02-28
  • 通讯作者: 田丽美 E-mail:tianmeili2007@163.com
  • 基金资助:
    国家自然科学基金项目(31772330);黑龙江八一农垦大学科研团队、平台支持计划项目(TDJH202004)

Cytological Observation of Fruit Peduncle Abscission Zone and Preliminary Mapping of Mature Fruit Abscission AL3 gene in Melon

SHENG Yunyan1, YANG Limin1, DAI Dongyang1, ZHANG Jiaxin1, WANG Ling1, WANG Di2, CAI Yi1, TIAN Limei1,*()   

  1. 1College of Horticulture and Landscape Architecture,Heilongjiang Bayi Agricultural University,Daqing,Heilongjiang 163319,China
    2Daqing Branch of Heilongjiang Academy of Agricultural Sciences,Daqing,Heilongjiang 163310,China
  • Received:2021-05-11 Revised:2021-11-03 Online:2022-02-25 Published:2022-02-28
  • Contact: TIAN Limei E-mail:tianmeili2007@163.com

摘要:

以甜瓜果实成熟不脱蒂材料M2-10为母本,易脱蒂材料ZT091为父本,配制杂交组合,获得F2、F3、F4及回交群体,利用6世代群体分析脱蒂性状的遗传规律,显示由两对基因控制,不脱蒂与脱蒂分离比符合两对互补基因遗传规律。对亲本果实成熟期果柄与果肉连接处离区组织石蜡切片及电镜扫描观察结果表明,亲本间离区细胞存在差异,ZT091果柄离区细胞体积增大、排列松散,细胞间隙较大。利用SLAF-BSA测序,对83-F3家系单基因分离群体开展控制脱蒂性状的AL3基因初步定位研究,将其定位在第8号染色体10 686 821 ~ 11 042 074 bp区间,覆盖0.355 Mb。通过亲本重测序数据挖掘SNP位点,设计CAPs标记,利用F4群体将AL3最后定位在8号染色体约64.7 kb区间内(10 774 778 ~ 10 839 486 bp),包含10个候选基因。

关键词: 甜瓜, 脱落, 细胞学观察, 基因定位

Abstract:

The F2,F3,F4 and backcross populations derived from a cross between M2-10 (none-mature fruit abscission,NMFA)and ZT091(mature fruit abscission,MFA)was used to study the cytological observation of abscission zone and gene mapping of one of mature fruit abscission(MFA)gene(AL3).The analysis of genetic inheritance indicated that the MFA was controlled by two genes. Paraffin section and scanning electron microscopy observation of the parent fruit at the maturity stage showed that the cells in the abscission zone of peduncle of ZT091 were larger in size,loosen arrangement and larger spaces between cells,there were significant difference between parental peduncle abscission zone. AL3 was primary mapped into a 0.355 Mb region(from 10 686 821 to 11 042 074 bp)on chromosome 8 with the strategy of SLAF-BSA using 83-F3 family only segregated with AL3. F4 family and CAPs markers were used for narrowing down the mapping region. Finally, AL3 was fined mapped into a 64.7 kb(from 10 774 778 to 10 839 486 bp)region with 10 annotated candidate genes.

Key words: melon, fruit abscission, cyotological observation, gene mapping

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