scholarly journals Development of a simultaneous detection method of DNA markers linked to four disease and pest resistance genes in potato using multiplex PCR

2010 ◽  
Vol 12 (1) ◽  
pp. 22-25
Author(s):  
Kazuyuki Mori ◽  
Kengo Ohbayashi ◽  
Seiji Tamiya ◽  
Yu Sakamoto ◽  
Nobuhiro Mukojima ◽  
...  
Euphytica ◽  
2011 ◽  
Vol 180 (3) ◽  
pp. 347-355 ◽  
Author(s):  
Kazuyuki Mori ◽  
Yu Sakamoto ◽  
Nobuhiro Mukojima ◽  
Seiji Tamiya ◽  
Takashi Nakao ◽  
...  

2016 ◽  
Vol 52 (5) ◽  
pp. 498-506 ◽  
Author(s):  
A. P. Yermishin ◽  
O. V. Svitoch ◽  
E. V. Voronkova ◽  
O. N. Gukasian ◽  
V. I. Luksha

2010 ◽  
Vol 46 (No. 2) ◽  
pp. 85-89 ◽  
Author(s):  
T. Sumíková ◽  
A. Hanzalová

Multiplex PCR was developed and optimized for simultaneous detection of wheat leaf rust resistance genes Lr26 and Lr37. The presence of the genes was analyzed in 21 winter wheat cultivars registered in the Czech Republic. Gene Lr37 was detected in four tested cultivars (Bakfis, Biscay, Nicol, Mulan), gene Lr26 occurred only in one cultivar (Etela) and three cultivars (Clarus, Orlando and Rapsodia) were found to carry both these genes. Data obtained by PCR markers were compared with results of greenhouse and field tests. Seedling reactions of cultivars possessing Lr26 to seven different leaf rust isolates conformed to the results obtained by the marker analysis, however, there were found some discrepancies in the detections of Lr37, which could be detected in greenhouse seedling tests only with difficulties.


Author(s):  
N.A. Kozub ◽  
I.A. Sozinov ◽  
A.Ya. Bidnyk ◽  
N.A. Demianova ◽  
Ya.B. Blume ◽  
...  

A combination of recombinant-inbred lines of the F6 generation from the cross B-16 ќ AR 7086 between lines with two wheat-rye translocations, 1BL/1RS from the Petkus and 1AL/1RS from the rye Insave, was developed. Using gliadin and secalin loci as genetic markers we identified recombinant arm 1RS in positions 1A and 1B in about 10% of lines. The rest of lines with the rye material may also carry recombinant 1RS, which can be identified with DNA markers. Lines with recombinant arm 1RS may serve as a source of new combination of rye genes for disease and pest resistance.


2019 ◽  
Vol 9 (13) ◽  
pp. 2688
Author(s):  
Kim ◽  
Kim ◽  
Lim ◽  
Choi ◽  
Lee

Cotton has been cultivated worldwide and is a useful crop for humans. However, all living modified organisms (LMOs), including living modified (LM) cotton, are not cultivated in South Korea and are imported from overseas. LM cotton imports are on the rise and most of the imported cotton is used as livestock feed. In particular, it is commonly used to feed Holstein breeds that produce milk, because cotton improves the quality of milk. However, as the cotton imports increase, the possibility of unintentional outflows in the distribution process also increases. Consequently, there is an increasing concern about unintentional release of LM cotton into the natural environment. Therefore, environmental monitoring and post-management of LMOs are very important steps. Recently, a total of 30 LM crop events were approved for LM cotton import in South Korea. A single detection method has been used to monitor individual events. However, a single method of detection for collected samples requires a large number of PCRs, with obvious disadvantages. Therefore, a simultaneous detection method was developed for 8 representative events (GHB119, GHB614, MON88913, MON15985, LLCOTTON25, MON1445, 281-3006, and MON531) in an effort to monitor 26 of them and facilitate the identification of LM cotton. The results suggest that our new multiplex PCR method may be useful for monitoring and post-management of LM cotton.


2019 ◽  
Vol 6 (2) ◽  
pp. 262-275
Author(s):  
Giovana Hashimoto Nakadomari ◽  
Amanda Carmen Charalo ◽  
Ana Claudia Lemes Pavan ◽  
Vanessa Kelly Capoia Vignoto ◽  
Ricardo Antonio Pilegi Sfaciotte ◽  
...  

A Staphylococcus Multiplex PCR system was developed for the simultaneous detection of the mecA, mecC, blaZ (resistance genes of b-lactam resistance) and PVL (pathogenicity factor gene), associated with an internal reaction control with the 16S rRNA gene. There were used primers described in the literature with and without modification and designed primers to standardize the hybridization and amplification temperature of distinct bands with 139 bp (mecC), 228 bp (16S), 313 bp (mecA), 408 bp (PVL) and 516 bp (blaZ) of molecular weight. The standardization was performed in ATCC strains and Staphylococcus schleiferiand tested in 56 strains of Staphylococcusspp. The 16S gene (internal control) was amplified in all samples, mecA gene was detected in two samples, mecA associated with mecC gene in one sample, mecA associated to the blaZ gene in 14 samples and the blaZ gene in 15 samples. No resistance genes were amplified in 24 samples. The PVL gene was not amplified in any of the samples tested.


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