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. 2017 Aug 29;8(4):e01314-17. doi: 10.1128/mBio.01314-17

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Copyright © 2017 Harari et al.

This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.

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FIG 2 — Cell fitness in wild-type strains with long telomeres. (A) Schematic cartoon representing the process of mating of haploid cells, followed by sporulation and tetrad dissection. (B) Telo-blot analysis of haploid meiotic products with long telomeres. (C) Relative doubling time measurements for untreated wild-type cells (BY4741) and haploid meiotic products of long telomeres in media consisting of either YPD (green bars) and YPD plus 5% ethanol (blue bars). For each candidate, doubling times in YPD media and in YPD–5% ethanol media are normalized according to the doubling time of BY4741 in YPD medium. (D) Relative doubling-time measurements for wild-type cells (BY4741) of normal telomere length and haploid meiotic products from a single tetrad in media consisting of either YPD (green bars) or YPD plus 5% ethanol (blue bars) (results were normalized as described for panel C).