Evidence map›Paper›PMID 29669733›Full record

ArticleGenetics2018

Evolution of DNAase I Hypersensitive Sites in MHC Regulatory Regions of Primates.

Yabin Jin, Rachel M Gittelman, Yueer Lu, Xiaohui Liu, Ming D Li, Fei Ling, Joshua M Akey

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2018. 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
1.2field-weighted citation impact, top 23% 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, 17 citations in OpenAlex.

  1. Article
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  3. Review
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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

7 authors at 5 institutions in 2 countries.

Yabin JinSchool of Biology and Biological Engineering, South China University of Technology, Guangzhou 510006, P. R. China.
Rachel M GittelmanDepartment of Genome Sciences, University of Washington, Seattle, Washington 98125.
Yueer LuSchool of Biology and Biological Engineering, South China University of Technology, Guangzhou 510006, P. R. China.
Xiaohui LiuInstitute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100094, P. R. China.
Ming D LiState Key Laboratory of Diagnosis and Treatment of Infectious Diseases, First Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou 310009, P. R. China.
Fei LingSchool of Biology and Biological Engineering, South China University of Technology, Guangzhou 510006, P. R. China fling@scut.edu.cn jakey@princeton.edu.ORCID 0000-0002-3640-4280
Joshua M AkeyDepartment of Genome Sciences, University of Washington, Seattle, Washington 98125 fling@scut.edu.cn jakey@princeton.edu.
South China University of Technology · CNUniversity of Washington · USFirst Affiliated Hospital Zhejiang University · CNInstitute of Plant Protection · CNSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It has been challenging to determine the disease-causing variant(s) for most major histocompatibility complex (MHC)-associated diseases. However, it is becoming increasingly clear that regulatory variation is pervasive and a fundamentally important mechanism governing phenotypic diversity and disease susceptibility. We gathered DNase I data from 136 human cells to characterize the regulatory landscape of the MHC region, including 4867 DNase I hypersensitive sites (DHSs). We identified thousands of regulatory elements that have been gained or lost in the human or chimpanzee genomes since their evolutionary divergence. We compared alignments of the DHS across six primates and found 149 DHSs with convincing evidence of positive and/or purifying selection. Of these DHSs, compared to neutral sequences, 24 evolved rapidly in the human lineage. We identified 15 instances of transcription-factor-binding motif gains, such as

Indexed as

Evolution, MolecularPolymorphism, Single NucleotidePromoter Regions, GeneticAnimalsCell LineDeoxyribonuclease IHumansMacacaMajor Histocompatibility ComplexNucleotide MotifsPan troglodytesQuantitative Trait LociSelection, GeneticTranscription FactorsDeoxyribonuclease ITranscription FactorsDNase I hypersensitive sitesGenomic SelectionGenPredmajor histocompatibility complexpositive selectionprimate genomepurifying selectionregulatory variationShared Data Resources

Identifiers

PMID29669733
PMCPMC5972428
OpenAlexW2799324862

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.