Frequent Meiotic Recombination Between the Ends of Truncated Chromosome Fragments of Saccharomyces cerevisiae

Corresponding author: Giora Simchen, Department of Genetics, The Hebrew University, Jerusalem 91904, Israel., simchen{at}vms.huji.ac.il (E-mail)

Communicating editor: M. LICHTEN

A single truncated chromosome fragment (TCF) in diploid cells undergoes frequent ectopic recombination during meiosis between markers located near the ends of the fragment. Tetrads produced by diploids with a single TCF show frequent loss of one of the two markers. This marker loss could result either from recombination of the TCF with one of the two copies of the chromosome from which it was derived or from ectopic recombination between the ends of the TCF. The former would result in shortening of a normal chromosome and lethality in one of the four spores. The high frequency of marker loss in tetrads with four viable spores supports recombination between the TCF ends as the main source of marker loss. Most of the spore colonies that display TCF marker loss contained a TCF with the same marker on both ends. Deletion of most of the pBR322 sequences distal to the marker at one of the subtelomeric regions of the TCF did not reduce the overall frequency of recombination between the ends, but affected the loss of one marker significantly more than the other. We suggest that the mechanism by which the duplication of one end marker and loss of the other occurs is based on association and recombination between the ends of the TCF.

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				A. B. Barton, Y. Su, J. Lamb, D. Barber, and D. B. Kaback A Function for Subtelomeric DNA in Saccharomyces cerevisiae Genetics, October 1, 2003; 165(2): 929 - 934. [Abstract] [Full Text] [PDF]