Evidence map›Paper›PMID 32759226›Full record

ArticleGenome research2020

Diploid genome architecture revealed by multi-omic data of hybrid mice.

Zhijun Han, Kairong Cui, Katarzyna Placek, Ni Hong, Chengqi Lin, Wei Chen, Keji Zhao, Wenfei Jin

Abstract read
In one paragraph

Article in Genome research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
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  8. Building Haplotype-Resolved 3D Genome Maps of Chicken Skeletal Muscle.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  9. Article
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  13. Review
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  15. Review
  16. Understanding three-dimensional chromatin organization in diploid genomes.Computational and structural biotechnology journal · 2021
    Review
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

8 authors.

Zhijun HanDepartment of Biology, Southern University of Science and Technology, Shenzhen, Guangdong 518055, China.
Kairong CuiSystems Biology Center, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.
Katarzyna PlacekSystems Biology Center, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.
Ni HongDepartment of Biology, Southern University of Science and Technology, Shenzhen, Guangdong 518055, China.
Chengqi LinInstitute of Life Sciences, Southeast University, Nanjing, Jiangsu 210096, China.
Wei ChenDepartment of Biology, Southern University of Science and Technology, Shenzhen, Guangdong 518055, China.
Keji ZhaoSystems Biology Center, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.
Wenfei JinDepartment of Biology, Southern University of Science and Technology, Shenzhen, Guangdong 518055, China.ORCID 0000-0002-0028-3739

Funding

Genome-wide mapping of histone modificationsZIAHL005801 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI ZHAO, KEJI · 2009 to 2025
$24.0M
6 · The paper itself

Abstract

Although mammalian genomes are diploid, previous studies extensively investigated the average chromatin architectures without considering the differences between homologous chromosomes. We generated Hi-C, ChIP-seq, and RNA-seq data sets from CD4 T cells of B6, Cast, and hybrid mice, to investigate the diploid chromatin organization and epigenetic regulation. Our data indicate that inter-chromosomal interaction patterns between homologous chromosomes are similar, and the similarity is highly correlated with their allelic coexpression levels. Reconstruction of the 3D nucleus revealed that distances of the homologous chromosomes to the center of nucleus are almost the same. The inter-chromosomal interactions at centromere ends are significantly weaker than those at telomere ends, suggesting that they are located in different regions within the chromosome territories. The majority of A|B compartments or topologically associated domains (TADs) are consistent between B6 and Cast. We found 58% of the haploids in hybrids maintain their parental compartment status at B6/Cast divergent compartments owing to

Indexed as

AnimalsCD4-Positive T-LymphocytesCell NucleusChimeraChromatinChromatin Assembly and DisassemblyChromosomesDiploidyEpigenesis, GeneticGenomeMiceMice, Inbred C57BLPolymorphism, Single NucleotideSequence Analysis, RNAChromatin

Identifiers

PMID32759226
PMCPMC7462080

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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.