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Zhenfang Wu

Researcher at Chinese Academy of Sciences

Publications -  16
Citations -  444

Zhenfang Wu is an academic researcher from Chinese Academy of Sciences. The author has contributed to research in topics: Origin of replication & Origin recognition complex. The author has an hindex of 9, co-authored 16 publications receiving 342 citations. Previous affiliations of Zhenfang Wu include Laboratory of Molecular Biology.

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Creating a functional single-chromosome yeast

TL;DR: A functional single-chromosome yeast from a Saccharomyces cerevisiae haploid cell containing sixteen linear chromosomes is created by successive end-to-end chromosome fusions and centromere deletions to demonstrate an approach to exploration of eukaryote evolution with respect to chromosome structure and function.
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Complete Genome Sequence of Haloarcula hispanica, a Model Haloarchaeon for Studying Genetics, Metabolism, and Virus-Host Interaction

TL;DR: The complete genome sequence of H. hispanica strain CGMCC 1.2049, consisting of two chromosomes and one megaplasmid is reported, which is significant for studying archaeal genetics, metabolism, and virus-host interactions.
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Diversity and evolution of multiple orc/cdc6 -adjacent replication origins in haloarchaea

TL;DR: A comparison of the origin-associated Orc/Cdc6 homologs and the corresponding predicted ORB elements revealed that the replication origins in a given haloarchaeon are quite diverse, while different halo archaea can share a few conserved origins.
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DNA replication origins in archaea

TL;DR: This review summarizes the research progress in understanding of archaeal replication origins with particular focus on the utilization, control and evolution of multiple replication origins in haloarchaea.
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Multiple replication origins with diverse control mechanisms in Haloarcula hispanica

TL;DR: The active replication origins in the three replicons of a halophilic archaeon, Haloarcula hispanica, are investigated by extensive gene deletion, DNA mutation and genome-wide marker frequency analyses, revealing that individual origins are specifically dependent on their co-located cdc6 genes and a single active origin/cdc6 pairing is essential and sufficient for each replicon.