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1.
Electron. j. biotechnol ; 46: 1-7, jul. 2020. ilus, graf, tab
Artigo em Inglês | LILACS | ID: biblio-1223252

RESUMO

BACKGROUND: Fragrance is one of the most important quality traits in rice, and the phenotype is attributed to the loss-of-function betaine aldehyde dehydrogenase (BADH2) gene. At least 12 allelic variations of BADH2 have been identified, and some of these have been applied to rice fragrance breeding using traditional molecular markers and Sanger sequencing techniques. However, these traditional methods have several limitations, such as being very expensive, imprecise, inefficient, and having security issues. Thus, a new molecular marker technology must be developed to improve rice fragrance breeding. RESULTS: In this study, more than 95% of the cultivated fragrant rice varieties belonged to a 7-bp deletion in exon 2 (badh2-E2) or an 8-bp deletion and 3-bp variation in exon 7 (badh2-E7). Both allelic variations resulted in the loss of function of the badh2 gene. We developed two novel SNP molecular markers, SNP_badh2-E2 and SNP_badh2- E7, related to the alleles. Their genotype and phenotype were highly cosegregated in the natural variation of rice accessions, with 160 of the 164 fragrant rice varieties detected with the two markers. These markers cosegregated with the fragrance phenotype in the F2 population. CONCLUSIONS: Two functional SNP molecular markers of badh2-E2 and badh2-E7 allelic variations were developed. These functional SNP molecular markers can be used for genotype and genetic improvement of rice fragrance through marker-assisted selection and will significantly improve the efficiency of fragrant rice breeding and promote commercial molecular breeding of rice in the future.


Assuntos
Oryza/enzimologia , Oryza/genética , Betaína-Aldeído Desidrogenase/metabolismo , Marcadores Genéticos , Alelos , Técnicas de Genotipagem/métodos , Genótipo , Odorantes
2.
Chinese Journal of Biotechnology ; (12): 329-339, 2012.
Artigo em Chinês | WPRIM | ID: wpr-304489

RESUMO

Plant betaine aldehyde dehydrogenase (BADH) is a physiologically important enzyme in response to salt or drought stress. In this study, two BADH genes (PeBADH1 and PeBADH2) were cloned from Populus euphratica. Both PeBADH1 and PeBADH2 genes encode the proteins of 503 amino acid residues, with a calculated molecular mass of 54.93 kDa and 54.90 kDa, respectively. Reverse transcription PCR showed the divergence of expression pattern between the PeBADH1 and PeBADH2 genes in P. euphratica. The recombinant PeBADH1 and PeBADH2 proteins were overexpressed in E. coli, and purified by Ni-affinity chromatography. The PeBADH2 protein had 1.5-fold higher enzymatic activity towards the substrate aldehyde than PeBADH1 protein. The PeBADH1 protein revealed higher thermal stability than PeBADH2 protein. These results indicated obvious functional divergence between the PeBADH1 and PeBADH2 genes.


Assuntos
Sequência de Aminoácidos , Betaína-Aldeído Desidrogenase , Genética , Clonagem Molecular , Escherichia coli , Genética , Metabolismo , Regulação da Expressão Gênica de Plantas , Fisiologia , Dados de Sequência Molecular , Proteínas de Plantas , Química , Genética , Populus , Genética , Isoformas de Proteínas , Química , Metabolismo , Proteínas Recombinantes , Genética , Especificidade por Substrato
3.
Chinese Journal of Biotechnology ; (12): 1464-1469, 2008.
Artigo em Chinês | WPRIM | ID: wpr-275362

RESUMO

The open reading frame of Spinacia oleracea Betaine Aldehyde Dehydrogenase (SoBADH) was retrieved from Spinacia oleracea and inserted into the Agrobacterium tumefaciens binary vector pBin438, which was driven by CaMV35S promoter, and produced the new binary vector pBSB. A. tumefaciens LBA4404 carrying this plasmid was used in genetic transformation of plants. Forty-five primary transgenic plants were detected by PCR and verified by the Southern blotting from 65 regenerated plants, of which 27 transgenic plants had only one copy of T-DNA. The Northern blotting and Western blotting analysis indicated that the SoBADH gene had been transcribed mRNA and expression protein in the transgenic cotton lines. The testing of SoBADH activity of transgenic plant leaves showed that the enzyme activity was much higher than that of the non-transgenic cotton. The growth of transgenic plants was well under the salinity and freezing stress, whereas the non-transgenic plant grew poorly and even died. Challenging with salinity, the height and fresh weight of transgenic plants was higher compared with those of non-transgenic plants. Under the freezing stress, the relative conductivity of leaf electrolyte leakage of the transgenic cotton lines was lower than that of non-transgenic plants. These results demonstrated that the SoBADH gene could over express in the exogenous plants, and could be used in genetic engineering for cotton stress resistance.


Assuntos
Adaptação Fisiológica , Betaína-Aldeído Desidrogenase , Genética , Temperatura Baixa , Gossypium , Genética , Plantas Geneticamente Modificadas , Genética , Salinidade , Spinacia oleracea , Genética , Estresse Fisiológico , Genética
4.
Chinese Journal of Biotechnology ; (12): 77-81, 2006.
Artigo em Chinês | WPRIM | ID: wpr-237021

RESUMO

In this study, the 5' -flanking proximal region of stress-induced gene encoding betaine aldehyde dehydrogenase was isolated by Adaptor-PCR and TAIL-PCR from halophyte Suaeda liaotungensis. 1993 bp sequence was obtained by sequencing. The transcription start site, which localized at 62 bases upstream of the start ATG, was predicted using TSSP-TCM program. The functional elements were analysed by PLACE programm. The SlBADH gene promoter contains the basic elements: TATA-box, CAAT-box, and stress-induced elements: salt responsed element, cold, dehydration, ABA and frozen responsed elements, WUN responsed elements and HSE. Obtaining the promoter of betaine aldehyde dehydrogenase gene from Suaeda liaotungensis provides a foundation for analyzing the stress-induced promoter elements, studying the relationship between structure and founction of the promoter, and investigating the molecular mechanism of BADH gene regulation.


Assuntos
Sequência de Bases , Betaína-Aldeído Desidrogenase , Genética , Chenopodiaceae , Genética , Temperatura Baixa , Regulação Enzimológica da Expressão Gênica , Regulação da Expressão Gênica de Plantas , Genes de Plantas , Dados de Sequência Molecular , Proteínas de Plantas , Genética , Regiões Promotoras Genéticas , Sais , Análise de Sequência de DNA , Sítio de Iniciação de Transcrição
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