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作 者:史培瑶 陈丽娟 孙昊杰 程梦豪 肖进[1] 袁春霞[1] 王秀娥[1] 王海燕[1] SHI Pei-Yao;CHEN Li-Juan;SUN Hao-Jie;CHENG Meng-Hao;XIAO Jin;YUAN Chun-Xia;WANG Xiu-E;WANG Hai-Yan(National Key Laboratory of Crop Genetics&Germplasm Enhancement and Utilization/Cytogenetics Institute/Collaborative Innovation Center for Modern Crop Production Co-sponsored by Province and Ministry(CIC-MCP),Nanjing Agricultural University,Nanjing 210095,Jiangsu,China)
机构地区:[1]南京农业大学作物遗传与种质创新国家重点实验室/细胞遗传研究所/现代作物生产省部共建协同创新中心,江苏南京210095
出 处:《作物学报》2023年第6期1455-1465,共11页Acta Agronomica Sinica
基 金:国家重点研发计划项目(2020YFE0202900);中央高校基本科研业务费(KYZZ2022003);江苏省现代农业产业技术体系(JATS[2021]463);江苏省种业振兴项目(JBGS[2021]006,013,047)资助
摘 要:栽培小麦近缘物种顶芒山羊草(Aegilops comosa,2n=2x=14,MM)是小麦改良的三级基因库。为准确鉴定顶芒山羊草M基因组染色体或染色体区段,本研究利用二代测序获得顶芒山羊草M基因组序列信息,从中鉴定出16条可能的特异卫星重复序列。根据这些序列设计12个寡核苷酸(oligo)探针进行oligo-FISH,结果表明,其中10个探针可在顶芒山羊草染色体上产生明显的杂交信号。对探针特异性分析发现,5个探针仅在顶芒山羊草染色体上产生杂交信号,在小麦染色体上未观察明显杂交信号,可作为顶芒山羊草特异探针鉴定小麦背景中的顶芒山羊草染色体。选择在顶芒山羊草染色体上信号分布丰富的3个探针(oligo-pAc89、oligo-pAc148、oligo-pAc225)组成探针套ONPS#AC1,结合利用本实验室根据小麦D亚基因组开发的寡核苷酸探针库,构建了顶芒山羊草的oligo-FISH核型。本研究构建的FISH核型可以准确识别顶芒山羊草各条染色体,为挖掘、转移和利用顶芒山羊草优异基因提供了快速准确的鉴定手段。Ae.comosa(Aegilops comosa,2n=2x=14,MM)is a tertiary gene bank for wheat improvement.In order to accurately identify the chromosomes of Ae.comosa M genome or the chromosome segments transferred into wheat,the next-generation sequencing information of Ae.comosa M genome were obtained.Based on the next-generation sequencing information of Ae.comosa M genome,12 oligonucleotide probes were designed for oligo-FISH analysis according to the 16 possible specific satellite repeats identified.The oligo-FISH results showed that ten of the probes could produce obvious hybridization signals on the chromosomes of Ae.comosa.The probe specificity analysis revealed that the five probes generated hybridization signals on the chromosomes of Ae.comosa,but there was no obvious hybridization signal on the chromosomes in wheat,which used as the specific probes to identify the chromosomes or chromosome segments of M genome in wheat background.Three probes(oligo-pAc89,oligo-pAc148,and oligo-pAc225)with abundant signal distribution on the chromosomes of Ae.comosa were selected to form a probe set named ONPS#AC1.Combined with the oligonucleotide probe library developed according to wheat D sub genome,the oligo-FISH karyotype of Ae.comosa was constructed,which can accurately identify each chromosome of the M genome,providing an important molecular cytogenetic basis for mining,transferring,and utilizing the excellent genes of Ae.comosa.
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