https://www.ahs.ac.cn/images/0513-353X/images/top-banner1.jpg|#|苹果
https://www.ahs.ac.cn/images/0513-353X/images/top-banner2.jpg|#|甘蓝
https://www.ahs.ac.cn/images/0513-353X/images/top-banner3.jpg|#|菊花
https://www.ahs.ac.cn/images/0513-353X/images/top-banner4.jpg|#|灵芝
https://www.ahs.ac.cn/images/0513-353X/images/top-banner5.jpg|#|桃
https://www.ahs.ac.cn/images/0513-353X/images/top-banner6.jpg|#|黄瓜
https://www.ahs.ac.cn/images/0513-353X/images/top-banner7.jpg|#|蝴蝶兰
https://www.ahs.ac.cn/images/0513-353X/images/top-banner8.jpg|#|樱桃
https://www.ahs.ac.cn/images/0513-353X/images/top-banner9.jpg|#|观赏荷花
https://www.ahs.ac.cn/images/0513-353X/images/top-banner10.jpg|#|菊花
https://www.ahs.ac.cn/images/0513-353X/images/top-banner11.jpg|#|月季
https://www.ahs.ac.cn/images/0513-353X/images/top-banner12.jpg|#|菊花

ACTA HORTICULTURAE SINICA ›› 2007, Vol. 34 ›› Issue (2): 311-316.

• 果树 • Previous Articles     Next Articles

Development of SSR Markers in Sweet Cherry Using Selectively Amplified Microsatellite

AI Cheng-xiang1, YU Xian-mei2, ZHANG Li-si1, WE IHai-rong1, XIN Li1, YUAN Ke-jun1, JIN Song-nan1,SUN Qing-rong1, and LIU Qing-zhong1*   

  1. (1Shandong Institute of Pom ology, Key Laboratory for Fruit Biotechnology Breeding of Shandong, Taipan, Shandong 271000,China; 2Institute of Environm ent and Plant Protection, Chinese Academy of Tropical Agricultural Sciences, Danzhou,Hainan 571737, China)
  • Received:2006-07-08 Revised:2006-12-26 Online:2007-04-25 Published:2007-04-25
  • Contact: LIU Qing-zhong

Abstract: A total of 100 sequenceswere isolated and cloned by SAM ( SelectivelyAmp li2
fiedMicrosatellite) and another one was obtained from the NCBI and EMBL databases. 82 SSR sequenceswere used to design the special primers at 77 loci from 69 fragments. Thirty-eight pairs of special primerswere synthesized, matchingwith 5′anchored degenerate SSR p rimer, to detect 36 SSR loci. 27 p rimer pairs amp lified clear and robust DNA fragment, of which nineteen pairs of SSR p rimers amp lified the corresponding SSR sequences and eight amplified the unexpected fragments. 24 polymorphic p rimer pairs were selected from the 27 p rimer pairs by using the genomic DNA of 27 sweet cherry germp lasm, and 24 locus-specific SSR markerswere obtained.

Key words: Prunus avium L., Germplasm, SSR markers, Selectively Amplified Microsatellite

CLC Number: