Development of loop-mediated isothermal amplification (LAMP)-based SNP markers for shelf-life in melon (Cucumis melo L.)

• Autorzy: S. Fukuta , Y. Mizukami , A. Ishida , M. Kanbe
• Języki publikacji: EN

Abstrakty

EN

In this study, LAMP markers linked to shelf-life in melon (Cucumis melo L.) were developed by converting a cleaved amplified polymorphic sequences (CAPS) marker (C2). The CAPS-PCR fragments from the long-shelf-life melon (O?3) and short-shelf-life melon (Nat-2) were cloned and sequenced to construct LAMP primers. A single nucleotide polymorphism (SNP) was identified between O?3 and Nat-2. LAMP primers were designed to detect the SNP. In the LAMP reaction to detect long-shelf-life melon, the turbidity of the templates using O?3, F1, homozygous long-shelf-life F2 lines and heterozygous long-shelf-life F2 lines started to increase after 40 min. In contrast, the turbidity of Nat-2 and homozygous short-shelf-life F2 lines did not increase even after 90 min. In the LAMP reaction to detect short-shelf-life melon, the turbidity of the templates using Nat-2, F1, homozygous short-shelf-life F2 lines and heterozygous long-shelf-life F2 lines started to increase after 40 min. But the turbidity of O?3 and homozygous long-shelf-life F2 lines did not increase after 90 min. This attests to the high reliability and usefulness of LAMP for marker-assisted selection.

Słowa kluczowe

EN

LAMP MARKER; MELON

• Czasopismo: Journal of Applied Genetics
• Rocznik: 2006
• Tom: 47
• Numer: 4
• Strony: 303-308

Twórcy

autor

S. Fukuta

autor

Y. Mizukami

autor

A. Ishida

autor

M. Kanbe

• Typ dokumentu: ARTICLE
• Bibliografia: S. Fukuta, Biotechnology Group, Aichi Pref. Agricultural Research Center, 1?1 Sagamine, Yazako, Nagakute, Aichi, 480?1193, Japan