Conditional genomic rearrangement by designed meiotic recombination using VDE (PI-SceI) in yeast. (Q53544906)

15 May 2018

title

Conditional genomic rearrangement by designed meiotic recombination using VDE (PI-SceI) in yeast. (English)

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15 May 2018

author

Tomoyuki Fukuda

series ordinal

1

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15 May 2018

author name string

Yoshikazu Ohya

series ordinal

2

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15 May 2018

Kunihiro Ohta

series ordinal

3

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15 May 2018

publication date

22 June 2007

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Molecular Genetics and Genomics

published in

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15 May 2018

volume

278

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issue

4

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page(s)

467-478

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15 May 2018

Partner choice during meiosis is regulated by Hop1-promoted dimerization of Mek1.

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HO endonuclease-induced recombination in yeast meiosis resembles Spo11-induced events.

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Protein splicing converts the yeast TFP1 gene product to the 69-kD subunit of the vacuolar H(+)-adenosine triphosphatase

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Recruitment of RecA homologs Dmc1p and Rad51p to the double-strand break repair site initiated by meiosis-specific endonuclease VDE (PI-SceI).

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Homing at an extragenic locus mediated by VDE (PI-SceI) in Saccharomyces cerevisiae

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Wild-type levels of Spo11-induced DSBs are required for normal single-strand resection during meiosis

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VDE-initiated intein homing in Saccharomyces cerevisiae proceeds in a meiotic recombination-like manner.

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Un ménage à quatre: the molecular biology of chromosome segregation in meiosis

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Clustering of meiotic double-strand breaks on yeast chromosome III

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Engineering of large numbers of highly specific homing endonucleases that induce recombination on novel DNA targets

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Molecular structure of a gene, VMA1, encoding the catalytic subunit of H(+)-translocating adenosine triphosphatase from vacuolar membranes of Saccharomyces cerevisiae

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A natural meiotic DNA break site in Schizosaccharomyces pombe is a hotspot of gene conversion, highly associated with crossing over

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Computational redesign of endonuclease DNA binding and cleavage specificity

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10.1007/S00438-007-0264-7

Identifiers

DOI

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15 May 2018

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15 May 2018