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Published online 28 April 2004

Nucleic Acids Research, 2004, Vol. 32, No. 8 2378-2385
© 2004 Oxford University Press

Meiosis-specific yeast Hop1 protein promotes synapsis of double-stranded DNA helices via the formation of guanine quartets

S. Anuradha and K. Muniyappa*

Department of Biochemistry, Indian Institute of Science, Bangalore 560012, India

*To whom correspondence should be addressed. Tel: +91 80 2394 2235/2360 0278; Fax: +91 80 2360 0814/0683; Email: kmbc{at}biochem.iisc.ernet.in

Received February 28, 2004; Revised March 22, 2004; Accepted April 1, 2004

In most eukaryotes, genetic exchange between paired homologs occurs in the context of a tripartite proteinaceous structure called the synaptonemal complex (SC). Genetic analyses have revealed that the genes encoding SC proteins are vital for meiotic chromosome pairing and recombination. However, the number, nature and/or the mechanism used by SC proteins to align chromosomes are yet to be clearly defined. Here, we show that Saccharomyces cerevisiae Hop1, a component of SC, was able to promote pairing of double-stranded DNA helices containing arrays of mismatched G/G sequences. Significantly, pairing was rapid and robust, independent of homology in the arms flanking the central G/G region, and required four contiguous guanine residues. Furthermore, data from truncated DNA double helices showed that 20 bp on either side of the 8 bp mismatched G/G region was essential for efficient synapsis. Methylation interference indicated that pairing between the two DNA double helices involves G quartets. These results suggest that Hop1 is likely to play a direct role in meiotic chromosome pairing and recombination by its ability to promote synapsis between double-stranded DNA helices containing arrays of G residues. To our knowledge, Hop1 is the first protein shown to promote synapsis of DNA double helices from yeast or any other organism.


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J. Biol. Chem.Home page
S. Anuradha and K. Muniyappa
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J. Biol. Chem., July 9, 2004; 279(28): 28961 - 28969.
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