scholarly journals Molecular-genetic testing of freshwater species and breeds of animals (fish, narrow-clawed crayfish, mollusks)

2018 ◽  
Vol 22 ◽  
pp. 126-131
Author(s):  
S. E. Dromashko ◽  
A. M. Slukvin ◽  
O. Yu. Koneva ◽  
A. A. Rouba ◽  
M. A. Sasinovich ◽  
...  

Aim. Description of the results of molecular genetic studies of a number of fish, narrow-clawed crayfish, and mollusk species. Methods. For the analysis, RAPD, SSR, and DNA-barcoding methods were used. Results. Unique RAPD amplicones were identified to differentiate Lahvinsky, Tremlyansky and Isobelinsky carp breeds. With the use of SSR markers, the Dniester-Dnieper and Kama population belonging to the sterlet, grown in two farms of Belarus, was established. An instruction on the application of molecular genetic analysis to establish the species belonging to meat and caviar of sturgeon species was developed. The species composition and genetic polymorphism in narrow-clawed crayfish in reservoirs of Brest and Gomel regions was estimated. The work on DNA-barcoding of mollusks has begun. Conclusions. Molecular-genetic passports of carp breeds of Belarusian breeding are compiled. The population belonging to sterlet is determined in two fish farms inBelarus. Instruction for the use of molecular genetic analysis to establish the species (population) belonging to the sturgeon fish and their products is introduced in the country and used for testing and certification of sturgeon products. For the Byelorussian Polesie region, it is established that the narrow-clawed crayfish in theGomel region reservoirs has the greatest genetic diversity. Keywords: molecular markers, carp, sturgeon, narrow-clawed crayfish, mollusks.

Author(s):  
А.Е. Яковлева ◽  
Д.А. Петухова ◽  
А.Л. Данилова ◽  
А.Л. Сухомясова ◽  
Н.Р. Максимова

В статье представлены результаты молекулярно-генетических исследованиий больных с множественной экзостозной хондродисплазией (МЭХД), причиной которой явилась редкая мутация в гене EXT2. Исследованы 65 больных с МЭХД и их родственников из 30 неродственных семей. Для молекулярно-генетического анализа было использовано массовое параллельное секвенирование и прямое секвенирование по Сэнгеру. У 16 больных из 4 семей с клиническим диагнозом МЭХД была выявлена редкая нонсенс-мутация c.751С>T в экзоне 5 гена EXT2 в гетерозиготном состоянии. Here we present molecular genetic studies of Yakut patients with hereditary multiple exostoses (HME), which caused by a rare mutation in the EXT2 gene. A total of 65 patients with clinical diagnosis of HME and their relatives from 30 unrelated families were examined. For molecular genetic analysis, massive parallel sequencing (MPS) and direct Sanger sequencing were used. In 16 patients from 4 families with a clinical diagnosis of HME, a rare heterozygous nonsense mutation c.751C> T was detected in exon 5 of the EXT2.


2016 ◽  
Vol 2 (3) ◽  
pp. 261-264 ◽  
Author(s):  
Anders Krogh Broendberg ◽  
Lisbeth Noerum Pedersen ◽  
Jens Cosedis Nielsen ◽  
Henrik Kjaerulf Jensen

1992 ◽  
Vol 174 (20) ◽  
pp. 6404-6410 ◽  
Author(s):  
R J Limberger ◽  
L L Slivienski ◽  
D B Yelton ◽  
N W Charon

Sign in / Sign up

Export Citation Format

Share Document