Evidence map›Paper›PMID 36131352›Full record

ArticleGenome biology2022

Genomics and epigenetics guided identification of tissue-specific genomic safe harbors.

Dewan Shrestha, Aishee Bag, Ruiqiong Wu, Yeting Zhang, Xing Tang, Qian Qi, Jinchuan Xing, Yong Cheng

Open access · goldAbstract read
In one paragraph

Article in Genome biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

14 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
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  8. Exogenous expression of ATP8, a mitochondrial encoded protein, from the nucleusMolecular therapy. Methods & clinical development · 2024
    Article
  9. Review
  10. Accelerating Diverse Cell-Based Therapies Through Scalable Design.Annual review of chemical and biomolecular engineering · 2024
    Review
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  12. 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

8 authors at 2 institutions in 1 country.

Dewan Shrestha *Department of Genetics, Genomics, and Informatics, College of Graduate Health Sciences, The University of Tennessee Health Science Center, Memphis, TN, USA.
Aishee Bag *Department of Genetics, Rutgers, The State University of New Jersey, Piscataway, NJ, USA.
Ruiqiong WuDepartment of Hematology, St. Jude Children's Research Hospital, Memphis, TN, USA.
Yeting ZhangDepartment of Genetics, Rutgers, The State University of New Jersey, Piscataway, NJ, USA.
Xing TangDepartment of Hematology, St. Jude Children's Research Hospital, Memphis, TN, USA.
Qian QiDepartment of Hematology, St. Jude Children's Research Hospital, Memphis, TN, USA.
Jinchuan XingDepartment of Genetics, Rutgers, The State University of New Jersey, Piscataway, NJ, USA. jinchuan.xing@rutgers.edu.
Yong ChengDepartment of Hematology, St. Jude Children's Research Hospital, Memphis, TN, USA. Yong.Cheng@STJUDE.ORG.ORCID 0000-0002-9314-0971
St. Jude Children's Research Hospital · USRutgers, The State University of New Jersey · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
Identification of causal non-coding variants in childhood genetic disordersR35GM133614 · NIGMS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHENG, YONG · 2019 to 2023
$2.2M
NCI NIH HHS P30 CA021765NIGMS NIH HHS R35 GM133614NIH HHS R35GM133614
6 · The paper itself

Abstract

backgroundGenomic safe harbors are regions of the genome that can maintain transgene expression without disrupting the function of host cells. Genomic safe harbors play an increasingly important role in improving the efficiency and safety of genome engineering. However, limited safe harbors have been identified.

resultsHere, we develop a framework to facilitate searches for genomic safe harbors by integrating information from polymorphic mobile element insertions that naturally occur in human populations, epigenomic signatures, and 3D chromatin organization. By applying our framework to polymorphic mobile element insertions identified in the 1000 Genomes project and the Genotype-Tissue Expression (GTEx) project, we identify 19 candidate safe harbors in blood cells and 5 in brain cells. For three candidate sites in blood, we demonstrate the stable expression of transgene without disrupting nearby genes in host erythroid cells. We also develop a computer program, Genomics and Epigenetic Guided Safe Harbor mapper (GEG-SH mapper), for knowledge-based tissue-specific genomic safe harbor selection.

conclusionsOur study provides a new knowledge-based framework to identify tissue-specific genomic safe harbors. In combination with the fast-growing genome engineering technologies, our approach has the potential to improve the overall safety and efficiency of gene and cell-based therapy in the near future.

Indexed as

EpigenomicsGenome, HumanChromatinEpigenesis, GeneticGenomicsHumansChromatinChromatin organizationEpigenomeGene therapyGenetic engineeringGenomic safe harborMobile genetic elements

Identifiers

PMID36131352
PMCPMC9490961
OpenAlexW4296709993

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.