Development of event-specific detection method for identification of insect resistant NIBGE-1601 cotton harboring double gene Cry1Ac-Cry2Ab construct

被引:5
作者
Asif, Muhammad [1 ]
Siddiqui, Hamid Anees [1 ,2 ]
Naqvi, Rubab Zahra [1 ]
Amin, Imran [1 ]
Asad, Shaheen [1 ]
Mukhtar, Zahid [1 ]
Bashir, Aftab [3 ]
Mansoor, Shahid [1 ]
机构
[1] Natl Inst Biotechnol & Genet Engn, Agr Biotechnol Div, Faisalabad, Pakistan
[2] Pakistan Inst Engn & Appl Sci, Nilore, Pakistan
[3] Forman Christian Coll, Dept Biol Sci, Lahore, Pakistan
关键词
POLYMERASE-CHAIN-REACTION; GENOME WALKING; PCR; PLANTS;
D O I
10.1038/s41598-021-82798-w
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Bt cotton expressing Cry1Ac is being cultivated in Pakistan. It has been observed that pink bollworm may have developed resistance against single Bt gene (Cry1Ac). For durable resistance, insect resistant NIBGE-1601 cotton harboring double gene Cry1Ac-Cry2Ab construct was developed. There was a need to characterize NIBGE-1601 event for intellectual property rights protection. The Presence of NIBGE Cry1Ac and NIBGE Cry2Ab genes was checked in NIBGE-1601 cotton plants through PCR, while there was no amplification using primers specific for Monsanto events (MON531, MON15985, MON1445). Using genome walking technology, NIBGE-601 event has been characterized. Event-specific primers of NIBGE-1601 were designed and evaluated to differentiate it from other cotton events mentioned above. NIBGE-1601 event detection primers are highly specific, therefore, can detect NIBGE 1601 event at different conditions using single or multiplex PCR. In the qualitative PCR, using NIBGE-1601 event specific primers, 0.05 ng was the limit of detection for NIBGE-1601double gene cotton genomic DNA. Thus event characterization and development of event-specific diagnostics will help in breeding new cotton varieties resistant to cotton bollworms.
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页数:9
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