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Kate Bailey

Researcher at Sainsbury Laboratory

Publications -  4
Citations -  402

Kate Bailey is an academic researcher from Sainsbury Laboratory. The author has contributed to research in topics: Albugo candida & Signal peptide. The author has an hindex of 4, co-authored 4 publications receiving 363 citations. Previous affiliations of Kate Bailey include University of Warwick & Norwich Research Park.

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Gene gain and loss during evolution of obligate parasitism in the white rust pathogen of Arabidopsis thaliana.

TL;DR: This work uses Illumina sequencing to define the genome, transcriptome, and gene models for the obligate biotroph oomycete and Arabidopsis parasite, Albugo laibachii, and suggests that evolution to progressively more intimate association between host and parasite results in reduced selection for retention of certain biosynthetic pathways, and particularly reduced selection of molybdopterin-requiring biosynthetics pathways.
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Molecular Cloning of ATR5Emoy2 from Hyaloperonospora arabidopsidis, an Avirulence Determinant That Triggers RPP5-Mediated Defense in Arabidopsis

TL;DR: The cloning and molecular characterization of the gene encoding ATR5(Emoy2) is described, an avirulence protein from the downy mildew pathogen Hyaloperonospora arabidopsidis isolate Emoy2, which triggers defense response in host lines expressing the functional RPP5 allele from Landsberg erecta (Ler-0).
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Evidence for suppression of immunity as a driver for genomic introgressions and host range expansion in races of Albugo candida, a generalist parasite

TL;DR: Sequential infection experiments show that infection by adapted races enables subsequent infection of hosts by normally non-infecting races, which facilitates introgression and the exchange of effector repertoires, and may enable the evolution of novel races that can undergo clonal population expansion on new hosts.
Posted ContentDOI

An improved assembly of the Albugo candida Ac2V genome reveals the expansion of the “CCG” class of effectors

TL;DR: In this paper, the authors re-sequenced the genome of isolate Ac2V using PacBio long reads and constructed an assembly augmented by Illumina reads, which revealed a dramatic 250% expansion in the CHxC effector class, which they redefined as "CCG" based on motif analysis.