Evidence map›Paper›PMID 38003233›Full record

ArticleInternational journal of molecular sciences2023

Trisomies Reorganize Human 3D Genome.

Irina V Zhegalova, Petr A Vasiluev, Ilya M Flyamer, Anastasia S Shtompel, Eugene Glazyrina, Nadezda Shilova, Marina Minzhenkova, Zhanna Markova, Natalia V Petrova, Erdem B Dashinimaev and 2 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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

12 authors at 6 institutions in 2 countries.

Irina V ZhegalovaCenter for Molecular and Cellular Biology, Skolkovo Institute of Science and Technology, 143026 Moscow, Russia.
Petr A VasiluevResearch Centre for Medical Genetics, 115522 Moscow, Russia.ORCID 0000-0002-8249-343X
Ilya M FlyamerFriedrich Miescher Institute for Biomedical Research, Maulbeerstrasse 66, 4058 Basel, Switzerland.
Anastasia S ShtompelDepartment of Molecular Biology, Faculty of Biology, M.V. Lomonosov Moscow State University, 119234 Moscow, Russia.ORCID 0009-0000-1582-4238
Eugene GlazyrinaMedical Genetic Center LLC Progen, 117630 Moscow, Russia.
Nadezda ShilovaResearch Centre for Medical Genetics, 115522 Moscow, Russia.ORCID 0000-0002-0641-1084
Marina MinzhenkovaResearch Centre for Medical Genetics, 115522 Moscow, Russia.ORCID 0000-0001-5458-0408
Zhanna MarkovaResearch Centre for Medical Genetics, 115522 Moscow, Russia.
Natalia V PetrovaLaboratory of Structural-Functional Organization of Chromosomes, Institute of Gene Biology, Russian Academy of Sciences, 119334 Moscow, Russia.
Erdem B DashinimaevCenter for Precision Genome Editing and Genetic Technologies for Biomedicine, Pirogov Russian National Research Medical University, 117997 Moscow, Russia.ORCID 0000-0002-5640-7139
Sergey V RazinDepartment of Molecular Biology, Faculty of Biology, M.V. Lomonosov Moscow State University, 119234 Moscow, Russia.ORCID 0000-0003-1976-8661
Sergey V UlianovDepartment of Molecular Biology, Faculty of Biology, M.V. Lomonosov Moscow State University, 119234 Moscow, Russia.
Research Centre for Medical Genetics · RULomonosov Moscow State University · RUFriedrich Miescher Institute · CHInstitute of Gene Biology · RUPirogov Russian National Research Medical University · RUSkolkovo Institute of Science and Technology · RU

Funding

Russian Ministry of Science and Higher Education 075-15-2021-1062
6 · The paper itself

Abstract

Trisomy is the presence of one extra copy of an entire chromosome or its part in a cell nucleus. In humans, autosomal trisomies are associated with severe developmental abnormalities leading to embryonic lethality, miscarriage or pronounced deviations of various organs and systems at birth. Trisomies are characterized by alterations in gene expression level, not exclusively on the trisomic chromosome, but throughout the genome. Here, we applied the high-throughput chromosome conformation capture technique (Hi-C) to study chromatin 3D structure in human chorion cells carrying either additional chromosome 13 (Patau syndrome) or chromosome 16 and in cultured fibroblasts with extra chromosome 18 (Edwards syndrome). The presence of extra chromosomes results in systematic changes of contact frequencies between small and large chromosomes. Analyzing the behavior of individual chromosomes, we found that a limited number of chromosomes change their contact patterns stochastically in trisomic cells and that it could be associated with lamina-associated domains (LAD) and gene content. For trisomy 13 and 18, but not for trisomy 16, the proportion of compacted loci on a chromosome is correlated with LAD content. We also found that regions of the genome that become more compact in trisomic cells are enriched in housekeeping genes, indicating a possible decrease in chromatin accessibility and transcription level of these genes. These results provide a framework for understanding the mechanisms of pan-genome transcription dysregulation in trisomies in the context of chromatin spatial organization.

Indexed as

Cell NucleusTrisomyChromatinGenetic TestingHumansInfant, NewbornTrisomy 13 SyndromeChromatinaneuploidychromatin spatial organizationEdwards syndromeHi-Cnuclear laminanucleus structurePatau syndrometranscription regulationtrisomy

Identifiers

PMID38003233
PMCPMC10671006
OpenAlexW4388446848

What Socratic holds

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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 Socratic graph.