1. Identification and expression analysis of genes associated with the early berry development in the seedless grapevine (Vitis vinifera L.) cultivar Sultanine
- Author
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Danielle Costenaro-da-Silva, Luís Fernando Revers, João Antonio Pêgas Henriques, Giancarlo Pasquali, Gisele Passaia, Rogério Margis, DANIELLE COSTENARO-DA-SILVA, UFRGS, GISELE PASSAIA, CNPUV (bolsista), JOÃO A. P. HENRIQUES, UFRGS, ROGÉRIO MARGIS, UFRGS, GIANCARLO PASQUALI, UFRGS, and LUIS FERNANDO REVERS, CNPUV.
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Candidate gene ,RDA ,In silico ,Plant Science ,Berry ,Expressão gênica ,Biology ,Uva de mesa ,PCR em tempo real ,Reference genes ,Botany ,Genetics ,Gene ,Biologia molecular ,Expressed sequence tag ,Identificação genética ,Viticultura ,fungi ,General Medicine ,Genética ,Phenotype ,Desenvolvimento da baga ,Uva sem semente ,Uva ,Representational difference analysis ,Agronomy and Crop Science - Abstract
Sultanine grapevine (Vitis vinifera L.) is one of the most important commercial seedless table-grape varieties and the main source of seedlessness for breeding programs around the world. Despite its commercial relevance, little is known about the genetic control of seedlessness in grapes, remaining unknown the molecular identity of genes responsible for such phenotype. Actually, studies concerning berry development in seedless grapes are scarce at the molecular level. We therefore developed a representational difference analysis (RDA) modified method named Bulk Representational Analysis of Transcripts (BRAT) in the attempt to identify genes specifically associated with each of the main developmental stages of Sultanine grapevine berries. A total of 2400 transcript-derived fragments (TDFs) were identified and cloned by RDA according to three specific developmental berry stages. After sequencing and in silico analysis, 1554 (64.75%) TDFs were validated according to our sequence quality cut-off. The assembly of these expressed sequence tags (ESTs) yielded 504 singletons and 77 clusters, with an overall EST redundancy of approximately 67%. Amongst all stage-specific cDNAs, nine candidate genes were selected and, along with two reference genes, submitted to a deeper analysis of their temporal expression profiles by reverse transcription-quantitative PCR. Seven out of nine genes proved to be in agreement with the stage-specific expression that allowed their isolation by RDA. Made available in DSpace on 2019-04-27T00:41:45Z (GMT). No. of bitstreams: 1 PlantScienceRevers2010.pdf: 520013 bytes, checksum: fe16ec2ebc986ea8d6298e5435908e08 (MD5) Previous issue date: 2010
- Published
- 2010
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