Abstract

In yeast, as in humans, telomere length varies among individuals and is controlled by multiple loci. In a quest to define the extent of variation in telomere length, we screened 112 wild-type Saccharomyces sensu stricto isolates. We found extensive telomere length variation in S. paradoxus isolates. This phenotype correlated with their geographic origin: European strains were observed to have extremely short telomeres (<150 bp), whereas American isolates had telomeres approximately three times as long (>400 bp). Insertions of a URA3 gene near telomeres allowed accurate analysis of individual telomere lengths and telomere position effect (TPE). Crossing the American and European strains resulted in F1 spores with a continuum of telomere lengths consistent with what would be predicted if many quantitative trait loci (QTLs) were involved in length maintenance. Variation in TPE is similarly quantitative but only weakly correlated with telomere length. Genotyping F1 segregants indicated several QTLs associated with telomere length and silencing variation. These QTLs include likely candidate genes but also map to regions where there are no known genes involved in telomeric properties. We detected transgressive segregation for both phenotypes. We validated by reciprocal hemizygosity that YKU80 and TLC1 are telomere-length QTLs in the two S. paradoxus subpopulations. Furthermore, we propose that sequence divergence within the Ku heterodimer generates negative epistasis within one of the allelic combinations (American-YKU70 and European-YKU80) resulting in very short telomeres.

Highlights

  • Telomeres are active nucleo-protein sites that constitute the ends of chromosomes in most eukaryotic species [1]

  • Telomere length is a complex trait that varies among individuals

  • We validated that naturally occurring sequence variations in YKU80 and TLC1, two genes previously shown to be important for telomere length maintenance, can explain part of the variation

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Summary

Introduction

Telomeres are active nucleo-protein sites that constitute the ends of chromosomes in most eukaryotic species [1]. Telomeric DNA is Grich and highly species specific in sequence. The telomeric DNA is bound by a number of proteins that together form a tight structure that effectively hides chromosome ends from DNA repair enzymes. Telomeric sequences are elegantly replenished by telomerase, a specialized reverse transcriptase. This process compensates for the loss of DNA from chromosome ends during DNA replication. Telomere length is both species and chromosome specific and appears to play an important role in the normal functioning of a cell. Telomerase (including its RNA template TLC1), Rap, yKu, and Mre complexes, Pif1p and Cdc13p are amongst the principal regulators of telomere length

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