دورية أكاديمية

Apple Autotetraploids with Enhanced Resistance to Apple Scab ( Venturia inaequalis ) Due to Genome Duplication-Phenotypic and Genetic Evaluation.

التفاصيل البيبلوغرافية
العنوان: Apple Autotetraploids with Enhanced Resistance to Apple Scab ( Venturia inaequalis ) Due to Genome Duplication-Phenotypic and Genetic Evaluation.
المؤلفون: Podwyszyńska M; Department of Applied Biology, Research Institute of Horticulture, Konstytucji 3 Maja 1/3 Street, 96-100 Skierniewice, Poland., Markiewicz M; Department of Applied Biology, Research Institute of Horticulture, Konstytucji 3 Maja 1/3 Street, 96-100 Skierniewice, Poland., Broniarek-Niemiec A; Department of Phytopathology, Research Institute of Horticulture, Konstytucji 3 Maja 1/3 Street, 96-100 Skierniewice, Poland., Matysiak B; Department of Applied Biology, Research Institute of Horticulture, Konstytucji 3 Maja 1/3 Street, 96-100 Skierniewice, Poland., Marasek-Ciolakowska A; Department of Applied Biology, Research Institute of Horticulture, Konstytucji 3 Maja 1/3 Street, 96-100 Skierniewice, Poland.
المصدر: International journal of molecular sciences [Int J Mol Sci] 2021 Jan 07; Vol. 22 (2). Date of Electronic Publication: 2021 Jan 07.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067 (Electronic) Linking ISSN: 14220067 NLM ISO Abbreviation: Int J Mol Sci Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Basel, Switzerland : MDPI, [2000-
مواضيع طبية MeSH: Fungal Genus Venturia/*genetics , Genome/*genetics , Malus/*genetics , Plant Diseases/*genetics, Fungal Genus Venturia/pathogenicity ; Gene Duplication/genetics ; Genotype ; Phenotype ; Plant Breeding ; Plant Diseases/microbiology ; Tetraploidy
مستخلص: Among the fungal diseases of apple trees, serious yield losses are due to an apple scab caused by Venturia inaequalis . Protection against this disease is based mainly on chemical treatments, which are currently very limited. Therefore, it is extremely important to introduce cultivars with reduced susceptibility to this pathogen. One of the important sources of variability for breeding is the process of polyploidization. Newly obtained polyploids may acquire new features, including increased resistance to diseases. In our earlier studies, numerous tetraploids have been obtained for several apple cultivars with 'Free Redstar' tetraploids manifesting enhanced resistance to apple scab. In the present study, tetraploids of 'Free Redstar' were assessed in terms of phenotype and genotype with particular emphasis on the genetic background of their increased resistance to apple scab. Compared to diploid plants, tetraploids (own-rooted plants) were characterized with poor growth, especially during first growing season. They had considerably shorter shoots, fewer branches, smaller stem diameter, and reshaped leaves. In contrast to own-rooted plants, in M9-grafted three-year old trees, no significant differences between diplo- and tetraploids were observed, either in morphological or physiological parameters, with the exceptions of the increased leaf thickness and chlorophyll content recorded in tetraploids. Significant differences between sibling tetraploid clones were recorded, particularly in leaf shape and some physiological parameters. The amplified fragment length polymorphism (AFLP) analysis confirmed genetic polymorphism of tetraploid clones. Methylation-sensitive amplification polymorphism (MSAP) analysis showed that the level of DNA methylation was twice as high in young tetraploid plants as in a diploid donor tree, which may explain the weaker vigour of neotetraploids in the early period of their growth in the juvenile phase. Molecular analysis showed that 'Free Redstar' cultivar and their tetraploids bear six Rvi genes ( Rvi5 , Rvi6 , Rvi8 , Rvi11 , Rvi14 and Rvi17 ). Transcriptome analysis confirmed enhanced resistance to apple scab of 'Free Redstar' tetraploids since the expression levels of genes related to resistance were strongly enhanced in tetraploids compared to their diploid counterparts.
References: Plant J. 2012 Jul;71(1):135-46. (PMID: 22381007)
Nucleic Acids Res. 1995 Nov 11;23(21):4407-14. (PMID: 7501463)
Nucleic Acids Res. 1996 Jul 1;24(13):2616-7. (PMID: 8692705)
New Phytol. 2010 Apr;186(1):5-17. (PMID: 20070540)
Mol Plant Pathol. 2019 May;20(5):626-640. (PMID: 30597698)
BMC Plant Biol. 2009 Jun 03;9:68. (PMID: 19493335)
Nat Prod Commun. 2015 Jan;10(1):209-18. (PMID: 25920246)
J Exp Bot. 2020 Mar 25;71(6):2085-2097. (PMID: 31844896)
Curr Opin Struct Biol. 2016 Dec;41:256-257. (PMID: 27884574)
Nat Struct Mol Biol. 2018 Sep;25(9):850-858. (PMID: 30190597)
Mol Gen Genet. 1999 Apr;261(3):439-46. (PMID: 10323223)
Int J Mol Sci. 2018 Feb 27;19(3):. (PMID: 29495448)
Theor Appl Genet. 2004 Nov;109(8):1702-9. (PMID: 15365630)
Genome. 2009 Feb;52(2):148-55. (PMID: 19234563)
Plant Physiol. 2002 Jan;128(1):21-9. (PMID: 11788749)
Hortic Res. 2017 Apr 05;4:17009. (PMID: 28435686)
Nature. 2010 Apr 1;464(7289):788-91. (PMID: 20360743)
J Proteome Res. 2019 Mar 1;18(3):826-840. (PMID: 30632760)
Mol Plant. 2013 May;6(3):686-703. (PMID: 23142764)
Curr Opin Genet Dev. 2018 Apr;49:1-7. (PMID: 29438956)
Indian J Microbiol. 2007 Dec;47(4):289-97. (PMID: 23100680)
Plant J. 2012 Aug;71(4):539-49. (PMID: 22449082)
Planta. 2016 Feb;243(2):281-96. (PMID: 26715561)
BMC Genet. 2014 Jan 06;15:2. (PMID: 24393618)
Int J Mol Sci. 2018 Jun 28;19(7):. (PMID: 29958430)
Sci Rep. 2016 May 24;6:26719. (PMID: 27216878)
Proc Biol Sci. 2007 Oct 7;274(1624):2393-7. (PMID: 17686733)
BMC Bioinformatics. 2005 Mar 21;6:62. (PMID: 15780134)
Annu Rev Phytopathol. 2011;49:391-413. (PMID: 21599495)
Curr Opin Plant Biol. 2009 Aug;12(4):459-64. (PMID: 19608451)
Microbiol Res. 2018 Jul - Aug;212-213:29-37. (PMID: 29853166)
Front Plant Sci. 2018 Mar 08;9:302. (PMID: 29568308)
Plant Dis. 2020 Aug;104(8):2074-2081. (PMID: 32525450)
Plant Cell. 2008 Mar;20(3):697-719. (PMID: 18375657)
Plant Physiol. 2016 Oct;172(2):1293-1305. (PMID: 27591188)
Plant Physiol. 2013 Oct;163(2):523-30. (PMID: 24014579)
Planta. 2016 Mar;243(3):635-44. (PMID: 26586177)
PLoS One. 2017 Sep 21;12(9):e0185288. (PMID: 28934340)
Cell. 2006 May 19;125(4):749-60. (PMID: 16713565)
Plant Physiol. 2016 Aug;171(4):2294-316. (PMID: 27288366)
Plant Sci. 2001 Jul;161(2):359-367. (PMID: 11448766)
Int J Mol Sci. 2012;13(8):10316-10335. (PMID: 22949863)
Philos Trans R Soc Lond B Biol Sci. 2014 Aug 5;369(1648):. (PMID: 24958924)
Hortic Res. 2020 Apr 1;7:57. (PMID: 32284869)
Plant Physiol. 2018 Feb;176(2):1143-1155. (PMID: 29269576)
معلومات مُعتمدة: Task No. 70 (2014-2020) Polish Ministry of Agriculture and Rural Development, Biological Progress
فهرسة مساهمة: Keywords: DNA methylation; Malus × domestica; Rvi genes; Venturia inaequalis; disease-resistance related genes; polyploidization
SCR Organism: Venturia inaequalis
تواريخ الأحداث: Date Created: 20210112 Date Completed: 20210330 Latest Revision: 20240806
رمز التحديث: 20240806
مُعرف محوري في PubMed: PMC7825683
DOI: 10.3390/ijms22020527
PMID: 33430246
قاعدة البيانات: MEDLINE
الوصف
تدمد:1422-0067
DOI:10.3390/ijms22020527