Genetic Characterization of the Fish Piaractus brachypomus by Microsatellites Derived from Transcriptome Sequencing

被引:15
作者
Jorge, Paulo H. [1 ]
Mastrochirico-Filho, Vito A. [1 ]
Hata, Milene E. [1 ]
Mendes, Natalia J. [1 ]
Ariede, Raquel B. [1 ]
de Freitas, Milena Vieira [1 ]
Vera, Manuel [2 ]
Porto-Foresti, Fabio [3 ]
Hashimoto, Diogo T. [1 ]
机构
[1] Sao Paulo State Univ, Univ Estadual Paulista Julio Mesquita Filho, Aquaculture Ctr, Jaboticabal, Brazil
[2] Univ Santiago Compostela, Vet Fac, Lugo, Spain
[3] Sao Paulo State Univ, Sch Sci, Bauru, Brazil
基金
巴西圣保罗研究基金会;
关键词
aquaculture; genetic structure; NGS; Pirapitinga; Serrasalmidae; SALMON SALMO-SALAR; INBREEDING DEPRESSION; COLOSSOMA-MACROPOMUM; POPULATION-STRUCTURE; DISEASE RESISTANCE; BREEDING PROGRAMS; HIGH-RESOLUTION; SPARUS-AURATA; GENOME; DIVERSITY;
D O I
10.3389/fgene.2018.00046
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The pirapitinga, Piaractus brachypomus (Characiformes, Serrasalmidae), is a fish from the Amazon basin and is considered to be one of the main native species used in aquaculture production in South America. The objectives of this study were: (1) to perform liver transcriptome sequencing of pirapitinga through NGS and then validate a set of microsatellite markers for this species; and (2) to use polymorphic microsatellites for analysis of genetic variability in farmed stocks. The transcriptome sequencing was carried out through the Roche/454 technology, which resulted in 3,696 non-redundant contigs. Of this total, 2,568 contigs had similarity in the non-redundant (nr) protein database (Genbank) and 2,075 sequences were characterized in the categories of Gene Ontology (GO). After the validation process of 30 microsatellite loci, eight markers showed polymorphism. The analysis of these polymorphic markers in farmed stocks revealed that fish farms from North Brazil had a higher genetic diversity than fish farms from Southeast Brazil. AMOVA demonstrated that the highest proportion of variation was presented within the populations. However, when comparing different groups (1: Wild; 2: North fish farms; 3: Southeast fish farms), a considerable variation between the groups was observed. The F-ST values showed the occurrence of genetic structure among the broodstocks from different regions of Brazil. The transcriptome sequencing in pirapitinga provided important genetic resources for biological studies in this non-model species, and microsatellite data can be used as the framework for the genetic management of breeding stocks in Brazil, which might provide a basis for a genetic pre-breeding programme.
引用
收藏
页数:12
相关论文
共 83 条
[61]   GenAlEx 6.5: genetic analysis in Excel. Population genetic software for teaching and research-an update [J].
Peakall, Rod ;
Smouse, Peter E. .
BIOINFORMATICS, 2012, 28 (19) :2537-2539
[62]   BOTTLENECK: A computer program for detecting recent reductions in the effective population size using allele frequency data [J].
Piry, S ;
Luikart, G ;
Cornuet, JM .
JOURNAL OF HEREDITY, 1999, 90 (04) :502-503
[63]   Accounting for genotype by environment interaction in economic appraisal of genetic improvement programs in common carp Cyprinus carpio [J].
Ponzoni, Raul W. ;
Nguyen, Nguyen Hong ;
Khaw, Hooi Ling ;
Nguyen Huu Ninh .
AQUACULTURE, 2008, 285 (1-4) :47-55
[64]  
Pritchard JK, 2000, GENETICS, V155, P945
[65]   RNA-Seq Technology and Its Application in Fish Transcriptomics [J].
Qian, Xi ;
Ba, Yi ;
Zhuang, Qianfeng ;
Zhong, Guofang .
OMICS-A JOURNAL OF INTEGRATIVE BIOLOGY, 2014, 18 (02) :98-110
[66]   Mining transcriptome sequences towards identifying adaptive single nucleotide polymorphisms in lake whitefish species pairs (Coregonus spp. Salmonidae) [J].
Renaut, Sebastien ;
Nolte, Arne W. ;
Bernatchez, Louis .
MOLECULAR ECOLOGY, 2010, 19 :115-131
[67]   ANALYZING TABLES OF STATISTICAL TESTS [J].
RICE, WR .
EVOLUTION, 1989, 43 (01) :223-225
[68]   GENEPOP′007:: a complete re-implementation of the GENEPOP software for Windows and Linux [J].
Rousset, Francois .
MOLECULAR ECOLOGY RESOURCES, 2008, 8 (01) :103-106
[69]  
Rozen S, 2000, Methods Mol Biol, V132, P365
[70]   An economic method for the fluorescent labeling of PCR fragments [J].
Schuelke, M .
NATURE BIOTECHNOLOGY, 2000, 18 (02) :233-234