Evidence map›Paper›PMID 40659358›Full record

ArticleGenetics2025

Long telomere inheritance through budding yeast sexual cycles.

Vasilisa Sidarava, Sarah Mearns, David Lydall

Erratum issuedAbstract read
In one paragraph

Article in Genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Vasilisa SidaravaBiosciences Institute, The Medical School, Framlington Place, Newcastle University, Newcastle upon Tyne, Tyne and Wear NE2 4HH, United Kingdom.ORCID 0009-0008-8106-3893
Sarah MearnsBiosciences Institute, The Medical School, Framlington Place, Newcastle University, Newcastle upon Tyne, Tyne and Wear NE2 4HH, United Kingdom.ORCID 0000-0002-6729-9858
David LydallBiosciences Institute, The Medical School, Framlington Place, Newcastle University, Newcastle upon Tyne, Tyne and Wear NE2 4HH, United Kingdom.ORCID 0000-0003-2478-085X

Funding

Darwin TrustNewcastle UniversityWellcome Trust
6 · The paper itself

Abstract

The ends of linear eukaryotic chromosomes are protected from being recognized as DNA double-strand breaks by telomeres, containing repetitive DNA sequences that bind specific proteins. In humans, mutations in telomere regulatory genes lead to short or long telomere syndromes. These syndromes often show genetic anticipation, where the disease has an earlier onset and a more severe manifestation in each new generation. Later generations inherit not only the mutation affecting telomere length, but also abnormal telomere length. Many aspects of telomere length homeostasis are conserved between mammals and yeast. Here, we explored telomere length inheritance patterns through the sexual cycle in yeast. Analysis of single telomeres, rather than bulk telomeres, shows that if haploid yeast with short telomeres mate with wild-type yeast, creating diploids, short telomere lengths rapidly normalize (within 30 cell divisions). However, long telomeres inherited from one parent can persist for more than 200 mitotic cell divisions. Long telomeres can also be transmitted through more than one round of meiosis, independently of mutations that cause long telomeres. These patterns, along with haploinsufficiency effects, show that even in yeast, there is a complex relationship between telomere length, telomere length inheritance, and mutations that affect telomere length. Our findings may have implications for families affected by telomere syndromes.

Indexed as

Saccharomyces cerevisiaeSaccharomycetalesTelomereTelomere HomeostasisHaploidyMeiosisMutationinheritancemeiosisSaccharomyces cerevisiaetelomere length

Identifiers

PMID40659358
PMCPMC12406008

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.