Oligonucleotides replacing the roles of repetitive sequences pAs1, pSc119.2, pTa-535, pTa71, CCS1, and pAWRC.1 for FISH analysis

被引:360
作者
Tang, Zongxiang [1 ]
Yang, Zujun [2 ]
Fu, Shulan [1 ]
机构
[1] Sichuan Agr Univ, State Key Lab Plant Breeding & Genet, Chengdu 611130, Sichuan, Peoples R China
[2] Univ Elect Sci & Technol China, Sch Life Sci & Technol, Chengdu 610054, Sichuan, Peoples R China
关键词
Chromosome identification; FISH; Oligonucleotide probe; Rye; Wheat; IN-SITU HYBRIDIZATION; RYE SECALE-CEREALE; NEOCENTRIC ACTIVITY; 5RL CHROMOSOME; DNA-SEQUENCES; WHEAT; TRITICALE; REGIONS; CENTROMERE; CULTIVARS;
D O I
10.1007/s13353-014-0215-z
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Hybrids derived from wheat (Triticum aestivum L.) x rye (Secale cereale L.) have been widely studied because of their important roles in wheat cultivar improvement. Repetitive sequences pAs1, pSc119.2, pTa-535, pTa71, CCS1, and pAWRC.1 are usually used as probes in fluorescence in situ hybridization (FISH) analysis of wheat, rye, and hybrids derived from wheat x rye. Usually, some of these repetitive sequences for FISH analysis were needed to be amplified from a bacterial plasmid, extracted from bacterial cells, and labeled by nick translation. Therefore, the conventional procedure of probe preparation using these repetitive sequences is time-consuming and labor-intensive. In this study, some appropriate oligonucleotide probes have been developed which can replace the roles of repetitive sequences pAs1, pSc119.2, pTa-535, pTa71, CCS1, and pAWRC.1 in FISH analysis of wheat, rye, and hybrids derived from wheat x rye. These oligonucleotides can be synthesized easily and cheaply. Therefore, FISH analysis of wheat and hybrids derived from wheat x rye using these oligonucleotide probes becomes easier and more economical.
引用
收藏
页码:313 / 318
页数:6
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