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The genome of Peronospora belbahrii reveals high heterozygosity, a low number of canonical effectors and CT-rich promoters.

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F20%3A73603314" target="_blank" >RIV/61989592:15310/20:73603314 - isvavai.cz</a>

  • Result on the web

    <a href="https://apsjournals.apsnet.org/doi/10.1094/MPMI-07-19-0211-R" target="_blank" >https://apsjournals.apsnet.org/doi/10.1094/MPMI-07-19-0211-R</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1094/MPMI-07-19-0211-R" target="_blank" >10.1094/MPMI-07-19-0211-R</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    The genome of Peronospora belbahrii reveals high heterozygosity, a low number of canonical effectors and CT-rich promoters.

  • Original language description

    Along with Plasmopara destructor, Peronosopora belbahrii has arguably been the economically most important newly emerging downy mildew pathogen of the past two decades. Originating from Africa, it has started devastating basil production throughout the world, most likely due to the distribution of infested seed material. Here, we present the genome of this pathogen and results from comparisons of its genomic features to other oomycetes. The assembly of the nuclear genome was around 35.4 Mbp in length, with an N-50 scaffold length of around 248 kbp and an L-50 scaffold count of 46. The circular mitochondrial genome consisted of around 40.1 kbp. From the repeat-masked genome, 9,049 protein-coding genes were predicted, out of which 335 were predicted to have extracellular functions, representing the smallest secretome so far found in peronosporalean oomycetes. About 16% of the genome consists of repetitive sequences, and, based on simple sequence repeat regions, we provide a set of microsatellites that could be used for population genetic studies of P. belbahrii. P. belbahrii has undergone a high degree of convergent evolution with other obligate parasitic pathogen groups, reflecting its obligate biotrophic lifestyle. Features of its secretome, signaling networks, and promoters are presented, and some patterns are hypothesized to reflect the high degree of host specificity in Peronospora species. In addition, we suggest the presence of additional virulence factors apart from classical effector classes that are promising candidates for future functional studies.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10608 - Biochemistry and molecular biology

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2020

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    MOLECULAR PLANT-MICROBE INTERACTIONS

  • ISSN

    0894-0282

  • e-ISSN

  • Volume of the periodical

    33

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    12

  • Pages from-to

    742-753

  • UT code for WoS article

    000531759000007

  • EID of the result in the Scopus database

    2-s2.0-85084153016