Evidence map›Paper›PMID 38011284›Full record

ArticlePLoS genetics2023

Spatial transcriptomics reveals novel genes during the remodelling of the embryonic human arterial valves.

Rachel Queen, Moira Crosier, Lorraine Eley, Janet Kerwin, Jasmin E Turner, Jianshi Yu, Ahlam Alqahtani, Tamilvendhan Dhanaseelan, Lynne Overman, Hannah Soetjoadi and 8 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 9 citations in OpenAlex.

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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

18 authors at 4 institutions in 2 countries.

Rachel QueenBioinformatics Support Unit, Faculty of Medical Sciences, Newcastle University, United Kingdom.
Moira CrosierHuman Developmental Biology Resource, Biosciences Institute, Faculty of Medical Sciences, Newcastle University, United Kingdom.
Lorraine EleyBiosciences Institute, Faculty of Medical Sciences, Newcastle University, United Kingdom.
Janet KerwinHuman Developmental Biology Resource, Biosciences Institute, Faculty of Medical Sciences, Newcastle University, United Kingdom.
Jasmin E TurnerHuman Developmental Biology Resource, Biosciences Institute, Faculty of Medical Sciences, Newcastle University, United Kingdom.
Jianshi YuDepartment of Pharmaceutical Sciences, University of Maryland School of Pharmacy, Baltimore, Maryland, United States of America.ORCID 0000-0002-4666-2435
Ahlam AlqahtaniBiosciences Institute, Faculty of Medical Sciences, Newcastle University, United Kingdom.
Tamilvendhan DhanaseelanHuman Developmental Biology Resource, Biosciences Institute, Faculty of Medical Sciences, Newcastle University, United Kingdom.
Lynne OvermanHuman Developmental Biology Resource, Biosciences Institute, Faculty of Medical Sciences, Newcastle University, United Kingdom.
Hannah SoetjoadiBiosciences Institute, Faculty of Medical Sciences, Newcastle University, United Kingdom.
Richard BaldockMRC Human Genetics Unit, Institute of Genetics and Cancer, Edinburgh University, United Kingdom.
Jonathan CoxheadGenomics Core Facility, Biosciences Institute, Faculty of Medical Sciences, Newcastle University, United Kingdom.
Veronika BoczonadiBioimaging Unit, Faculty of medical Sciences, Newcastle University, United Kingdom.
Alex LaudeBioimaging Unit, Faculty of medical Sciences, Newcastle University, United Kingdom.ORCID 0000-0002-3853-1187
Simon J CockellSchool of Biomedical, Nutritional and Sport Sciences, Faculty of Medical Sciences, Newcastle University, United Kingdom.ORCID 0000-0002-6831-9806
Maureen A KaneDepartment of Pharmaceutical Sciences, University of Maryland School of Pharmacy, Baltimore, Maryland, United States of America.
Steven LisgoHuman Developmental Biology Resource, Biosciences Institute, Faculty of Medical Sciences, Newcastle University, United Kingdom.ORCID 0000-0001-5186-3971
Deborah J HendersonHuman Developmental Biology Resource, Biosciences Institute, Faculty of Medical Sciences, Newcastle University, United Kingdom.ORCID 0000-0002-2705-5998
Newcastle University · GBUniversity of Maryland, Baltimore · USGenomics (United Kingdom) · GBInstitute of Genetics and Cancer · GB

Funding

British Heart Foundation RG/19/2/34256Wellcome Trust
6 · The paper itself

Abstract

Abnormalities of the arterial valves, including bicuspid aortic valve (BAV) are amongst the most common congenital defects and are a significant cause of morbidity as well as predisposition to disease in later life. Despite this, and compounded by their small size and relative inaccessibility, there is still much to understand about how the arterial valves form and remodel during embryogenesis, both at the morphological and genetic level. Here we set out to address this in human embryos, using Spatial Transcriptomics (ST). We show that ST can be used to investigate the transcriptome of the developing arterial valves, circumventing the problems of accurately dissecting out these tiny structures from the developing embryo. We show that the transcriptome of CS16 and CS19 arterial valves overlap considerably, despite being several days apart in terms of human gestation, and that expression data confirm that the great majority of the most differentially expressed genes are valve-specific. Moreover, we show that the transcriptome of the human arterial valves overlaps with that of mouse atrioventricular valves from a range of gestations, validating our dataset but also highlighting novel genes, including four that are not found in the mouse genome and have not previously been linked to valve development. Importantly, our data suggests that valve transcriptomes are under-represented when using commonly used databases to filter for genes important in cardiac development; this means that causative variants in valve-related genes may be excluded during filtering for genomic data analyses for, for example, BAV. Finally, we highlight "novel" pathways that likely play important roles in arterial valve development, showing that mouse knockouts of RBP1 have arterial valve defects. Thus, this study has confirmed the utility of ST for studies of the developing heart valves and broadens our knowledge of the genes and signalling pathways important in human valve development.

Indexed as

Bicuspid Aortic Valve DiseaseHeart Valve DiseasesAnimalsAortic ValveGene Expression ProfilingHumansMiceTranscriptome

Identifiers

PMID38011284
PMCPMC10703419
OpenAlexW4389042379

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.