scholarly journals DNA markers of AHAS1 gene for screening and identification of sunflower genotypes of hybrid origin

2018 ◽  
Vol 23 ◽  
pp. 126-130
Author(s):  
A. Ye. Solodenko

Aim. A molecular genetic study of sunflower F1 and F2 hybrids on a microsatellite markers of mutant AHAS1 gene associated with herbicide resistance was performed. The aim of the work was to screen of F1 and F2 sunflower hybrid populations with usage of DNA markers and identification of homozygous segregants containing of the gene for resistance to SU herbicides. Methods. It was used PCR amplification to detect alleles of microsatellite locus located within the mutant AHAS1 gene. Results. The possibility of identification of hybrid plants with different alleles of the AHAS1 gene was shown. The efficiency of the allele of 191 b. p. in the homo- and heterozygous state for marker selection of genotypes resistant to the herbicide of the sulfonylurea group was confirmed. 10 homozygous F2 plants of SURES-2 x OS 1019B and 18 homozygous F2 plants of SURES-2 x OS 1029B, which according to the genotype correspond to the donor line of the mutant AHAS1 gene, were obtained. Conclusions. F2 plants that are carriers of this gene in the homozygous state can be used as an initial material in breeding for the purpose of creating new inbred lines with genetically determined resistance to SU herbicides. Keywords: DNA markers, AHAS1 gene, sunflower, herbicides, resistance.

2020 ◽  
Vol 98 (3) ◽  
pp. 218-225
Author(s):  
J. A. Krupinova ◽  
N. G. Mokrysheva ◽  
N. Y. Kalinchenko ◽  
A. K. Eremkina ◽  
A. N. Polyakov ◽  
...  

Multiple endocrine neoplasia type 1 (MEN-1) is the most common cause of the hereditary type of primary hyperparathyroidism (PHPT). If a family type of PHPT is suspected, a dynamic monitoring of patients and their close relatives should be carried out throughout their lives. We present a clinical case of a family in which four members of a pedigree were diagnosed with familial isolated hyperparathyroidism (FIHP). The diagnosis was changed to MEN-1, because it appeared that one of the patients had pancreatic neuroendocrine tumor. Molecular genetic study of MEN1 by direct by means of Sanger sequencing revealed that six family members had a new heterozygous mutation in exon 9: s. 1252 G> T p. D418Y.


2018 ◽  
Vol 72 ◽  
pp. 100-106 ◽  
Author(s):  
Iñigo Espinosa ◽  
Antonio De Leo ◽  
Emanuela D'Angelo ◽  
Juan M. Rosa-Rosa ◽  
Marina Corominas ◽  
...  

2000 ◽  
Vol 13 (12) ◽  
pp. 1336-1346 ◽  
Author(s):  
Maureen J O'Sullivan ◽  
Michael Kyriakos ◽  
Xiaopei Zhu ◽  
Mark R Wick ◽  
Paul E Swanson ◽  
...  

2003 ◽  
Vol 25 (5) ◽  
pp. 362-366 ◽  
Author(s):  
Harumi Saijo ◽  
Harumi Nakayama ◽  
Takanori Ezoe ◽  
Katsuhito Araki ◽  
Sui Sone ◽  
...  

2005 ◽  
Vol 138 (2) ◽  
pp. 715-733 ◽  
Author(s):  
Amy Baldwin ◽  
Anthony Wardle ◽  
Ramesh Patel ◽  
Penny Dudley ◽  
Soon Ki Park ◽  
...  

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