Evidence map›Paper›PMID 31728160›Full record

ArticleBioData mining2019

Screening for mouse genes lost in mammals with long lifespans.

Lev I Rubanov, Andrey G Zaraisky, Gregory A Shilovsky, Alexandr V Seliverstov, Oleg A Zverkov, Vassily A Lyubetsky

Open access · goldAbstract read
In one paragraph

Article in BioData mining, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.2field-weighted citation impact, top 46% of its field
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

5 citing papers in PubMed, 14 citations in OpenAlex.

  1. The Change Rate of theBiology · 2024
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  2. Towards a Unitary Hypothesis of Alzheimer's Disease Pathogenesis.Journal of Alzheimer's disease : JAD · 2024
    Article
  3. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Lev I Rubanov1Institute for Information Transmission Problems of the Russian Academy of Sciences (Kharkevich Institute) IITP RAS, 19 build. 1 Bolshoy Karetny per., Moscow, 127051 Russia.ORCID 0000-0003-3012-2589
Andrey G Zaraisky2Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences (IBCH RAS) 16/10, Miklukho-Maklaya str., Moscow, 117997 Russia.
Gregory A Shilovsky1Institute for Information Transmission Problems of the Russian Academy of Sciences (Kharkevich Institute) IITP RAS, 19 build. 1 Bolshoy Karetny per., Moscow, 127051 Russia.
Alexandr V Seliverstov1Institute for Information Transmission Problems of the Russian Academy of Sciences (Kharkevich Institute) IITP RAS, 19 build. 1 Bolshoy Karetny per., Moscow, 127051 Russia.
Oleg A Zverkov1Institute for Information Transmission Problems of the Russian Academy of Sciences (Kharkevich Institute) IITP RAS, 19 build. 1 Bolshoy Karetny per., Moscow, 127051 Russia.
Vassily A Lyubetsky1Institute for Information Transmission Problems of the Russian Academy of Sciences (Kharkevich Institute) IITP RAS, 19 build. 1 Bolshoy Karetny per., Moscow, 127051 Russia.
Institute for Information Transmission Problems · RUInstitute of Bioorganic Chemistry · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGerontogenes include those that modulate life expectancy in various species and may be the actual longevity genes. We believe that a long (relative to body weight) lifespan in individual rodent and primate species can be due, among other things, to the loss of particular genes that are present in short-lived species of the same orders. These genes can also explain the widely different rates of aging among diverse species as well as why similarly sized rodents or primates sometimes have anomalous life expectancies (e.g., naked mole-rats and humans). Here, we consider the gene loss in the context of the prediction of Williams' theory that concerns the reallocation of physiological resources of an organism between active reproduction (r-strategy) and self-maintenance (K-strategy). We have identified such lost genes using an original computer-aided approach; the software considers the loss of a gene as disruptions in gene orthology, local gene synteny or both.

resultsA method and software identifying the genes that are absent from a predefined

conclusionsThe method and program, which were applied here to screen for gene losses that can accompany increased lifespan, were also applied to study reduced regenerative capacity and development of the telencephalon, neoteny, etc. Some of these results have been carefully tested experimentally. Therefore, we assume that the method is widely applicable.

Indexed as

AgingGene lossGerontologyIn silico analysisLifespanLongevitySynteny

Identifiers

PMID31728160
PMCPMC6842137
OpenAlexW2986963862

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.