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Single Nuclei Trans...
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Cavalli, MarcoUppsala universitet,Medicinsk genetik och genomik,Science for Life Laboratory, SciLifeLab
(författare)
Single Nuclei Transcriptome Analysis of Human Liver with Integration of Proteomics and Capture Hi-C Bulk Tissue Data
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LIBRIS-ID:oai:DiVA.org:uu-393431
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https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-393431URI
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Språk:engelska
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Sammanfattning på:engelska
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Ämneskategori:ref swepub-contenttype
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Ämneskategori:art swepub-publicationtype
Anmärkningar
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The liver is the largest solid organ and a primary metabolic hub. In recent years, intact cell nuclei were used to perform single-nuclei RNA-seq (snRNA-seq) for tissues difficult to dissociate and for flash-frozen archived tissue samples to discover unknown and rare cell sub-populations. In this study, we performed snRNA-seq of a liver sample to identify sub-populations of cells based on nuclear transcriptomics. In 4,282 single nuclei we detected on average 1,377 active genes and we identified seven major cell types. We integrated data from 94,286 distal interactions (p<0.05) for 7,682 promoters from a targeted chromosome conformation capture technique (HiCap) and mass spectrometry (MS) proteomics for the same liver sample. We observed a reasonable correlation between proteomics and in silico bulk snRNA-seq (r=0.47) using tissue-independent gene-specific protein abundancy estimation factors. We specifically looked at genes of medical importance. The DPYD gene is involved in the pharmacogenetics of fluoropyrimidines toxicity and some of its variants are analyzed for clinical purposes. We identified a new putative polymorphic regulatory element, which may contribute to variation in toxicity. Hepatocellular carcinoma (HCC) is the most common type of primary liver cancer and we investigated all known risk genes. We found a complex regulatory network for the SLC2A2 gene with 16 candidate enhancers. Three of them harbor somatic motif breaking and other mutations in HCC in the Pan Cancer Analysis of Whole Genomes dataset and are candidates to contribute to malignancy. Our results highlight the potential of a multi-omics approach in the study of human diseases.
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Biuppslag (personer, institutioner, konferenser, titlar ...)
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Diamanti, Klev,1987-Uppsala universitet,Beräkningsbiologi och bioinformatik(Swepub:uu)kledi204
(författare)
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Pan, GangUppsala universitet,Medicinsk genetik och genomik(Swepub:uu)ganpa561
(författare)
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Rapolas, SpalinskasScience for Life Laboratory, Division of Gene Technology, KTH Royal Institute of Technology
(författare)
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Kumar, ChanchalTranslational Science & Experimental Medicine, Early Cardiovascular, Renal and Metabolism, 12 BioPharmaceuticals R&D, AstraZeneca; Karolinska Institutet/AstraZeneca Integrated CardioMetabolic Center (KI/AZ ICMC), Department of Medicine
(författare)
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Deshmukh, Atul ShahajiNovo Nordisk Foundation Center for Protein Research, Proteomics Program, Clinical Proteomics Group
(författare)
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Mann, MatthiasNovo Nordisk Foundation Center for Protein Research, Proteomics Program, Clinical Proteomics Group
(författare)
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Sahlén, PelinScience for Life Laboratory, Division of Gene Technology, KTH Royal Institute of Technology
(författare)
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Komorowski, JanUppsala universitet,Science for Life Laboratory, SciLifeLab,Beräkningsbiologi och bioinformatik(Swepub:uu)jakom133
(författare)
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Wadelius, Claes,1955-Uppsala universitet,Science for Life Laboratory, SciLifeLab,Medicinsk genetik och genomik(Swepub:uu)claeswad
(författare)
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Uppsala universitetMedicinsk genetik och genomik
(creator_code:org_t)
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Cavalli, Marco
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Diamanti, Klev, ...
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Pan, Gang
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Rapolas, Spalins ...
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Kumar, Chanchal
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Deshmukh, Atul S ...
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Mann, Matthias
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Sahlén, Pelin
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Komorowski, Jan
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