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Cena A., Koz?owska E., P?ochocka D., et al. (2008) The F658G substitution in Saccharomyces cerevisiae cohesin Irr1/Scc3 is semidominant in the diploid and disturbs mitosis, meiosis and the cell cycle. European Journal of Cell Biology, 87, 8318-8344. doi:10.1016/j.ejcb.2008.05.002

has been cited by the following article:

• TITLE: Irr1/Scc3 cohesin interacts with Rec8 in meiotic prophase of Saccharomyces cerevisiae

  AUTHORS: Agata Cena, Piotr Kowalec, Danuta Płochocka, Anna Kurlandzka

  KEYWORDS: Irr1/Scc3; Cohesin; Rec8; Meiosis; Saccharomyces cerevisiae

  JOURNAL NAME: Open Journal of Genetics, Vol.2 No.1, March 2, 2012

  ABSTRACT: The meiotic cohesin complex of S. cerevisiae shares with the mitotic one the Irr1/Scc3, Smc1, and Smc3 subunits, while the meiosis-specific subunit Rec8 replaces mitotic subunit Scc1/Mcd1. We noticed earlier that the irr1-1 mutation (F658G) severely affected meiosis. The irr1 1/IRR1 cells were entering meiosis before having completed mitotic cell division. Using meiotic two-hybrid assay and co-immunoprecipitation we show that in cells arrested in pachytene due to a lack of a gene-regulatory factor Ndt80, the Irr1 protein interacts with Rec8p and the irr1-1 mutation abolishes this interaction. These findings indicate an important role of Irr1p in early stages of meiosis.