Genetic diversity of Asian rice gall midge based on mtCOI gene sequences and identification of a novel resistance locus gm12 in rice cultivar MN62M

2020 ◽  
Vol 47 (6) ◽  
pp. 4273-4283
Author(s):  
P. Leelagud ◽  
S. Kongsila ◽  
P. Vejchasarn ◽  
K. Darwell ◽  
Y. Phansenee ◽  
...  
2011 ◽  
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pp. 2842-2852 ◽  
Author(s):  
Deepak Kumar Sinha ◽  
Mulagondla Lakshmi ◽  
Ghanta Anuradha ◽  
Shaik J. Rahman ◽  
Ebrahimali A. Siddiq ◽  
...  

Genetica ◽  
2017 ◽  
Vol 145 (1) ◽  
pp. 37-49 ◽  
Author(s):  
Solene Janique ◽  
Wantana Sriratanasak ◽  
Kulchana Ketsuwan ◽  
Jirapong Jairin ◽  
Ekgachai Jeratthitikul

Genome ◽  
2001 ◽  
Vol 44 (6) ◽  
pp. 947-954 ◽  
Author(s):  
Susanta K Behura ◽  
Suresh Nair ◽  
Madan Mohan

In an effort to study genome diversity within and between the Indian biotypes of the Asian rice gall midge, Orseolia oryzae, a major insect pest of rice, we made use of mariner transposable element integration site polymorphisms. Using degenerate primers, the design of which is based on mariner sequences, we amplified a ca. 450 bp mariner sequence from the rice gall midge. The mariner sequence showed homology with that of a mariner element isolated from the Hessian fly, Mayetiola destructor, a major dipteran pest of wheat. Southern hybridization, using this mariner fragment as a probe, revealed that the mariner elements are moderately to highly repetitive in the rice gall midge genome. Based on the sequence information of this 450-bp PCR-amplified fragment, outward-directed primers were designed and used in an inverse PCR (iPCR) to amplify the DNA flanking the conserved regions. To study the regions flanking the mariner integration sites, we employed a novel PCR-based approach: a combination of sequence specific amplification polymorphism (SSAP) and amplified fragment length polymorphism (AFLP). The outward-directed mariner-specific primer was used in combination with adapter-specific primers with 1–3 selective nucleotides at their 3' ends. The amplification products were resolved on an agarose gel, Southern-transferred onto nylon membranes, and probed with the iPCR fragment. Results revealed biotype-specific polymorphisms in the regions flanking the mariner integration sites, suggesting that mariner elements in the rice gall midge may be fixed in a biotype-specific manner. The implications of these results are discussed in the context of biotype differentiation.Key words: DNA fingerprinting, inverse PCR (iPCR), Oryza sativa, rice pest, transposon.


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