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  1. Book: RNA bioinformatics

    Picardi, Ernesto

    (Methods in molecular biology ; 2284 ; Springer protocols)

    2021  

    Author's details edited by Ernesto Picardi
    Series title Methods in molecular biology ; 2284
    Springer protocols
    Collection
    Language English
    Size xiv, 581 Seiten, Illustrationen, Diagramme
    Edition Second edition
    Publisher Humana Press
    Publishing place New York, NY
    Publishing country United States
    Document type Book
    HBZ-ID HT020901446
    ISBN 978-1-0716-1306-1 ; 978-1-0716-1309-2 ; 9781071613078 ; 1-0716-1306-5 ; 1-0716-1309-X ; 1071613073
    Database Catalogue ZB MED Medicine, Health

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  2. Book: RNA editing

    Picardi, Ernesto / Pesole, Graziano

    methods and procotols

    (Methods in molecular biology ; 2181 ; Springer protocols)

    2021  

    Author's details edited by Ernesto Picardi, Graziano Pesole
    Series title Methods in molecular biology ; 2181
    Springer protocols
    Collection
    Language English
    Size XV, 352 Seiten, Illustrationen
    Publisher Humana Press
    Publishing place New York, NY
    Publishing country United States
    Document type Book
    HBZ-ID HT020553302
    ISBN 978-1-0716-0786-2 ; 1-0716-0786-3
    Database Catalogue ZB MED Medicine, Health

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  3. Book: RNA bioinformatics

    Picardi, Ernesto

    (Methods in molecular biology ; 1269 ; Springer protocols)

    2015  

    Author's details ed. by Ernesto Picardi
    Series title Methods in molecular biology ; 1269
    Springer protocols
    Collection
    Language English
    Size XII, 415 S. : Ill., graph. Darst.
    Publisher Humana Press
    Publishing place New York u.a.
    Publishing country United States
    Document type Book
    HBZ-ID HT018531058
    ISBN 978-1-4939-2290-1 ; 1-4939-2290-4 ; 978-1-4939-4644-0 ; 9781493922918 ; 1-4939-4644-7 ; 1493922912
    Database Catalogue ZB MED Medicine, Health

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  4. Article ; Online: Correction to: RNA Bioinformatics.

    Picardi, Ernesto

    Methods in molecular biology (Clifton, N.J.)

    2021  Volume 2284, Page(s) C1

    Language English
    Publishing date 2021-08-02
    Publishing country United States
    Document type Journal Article ; Published Erratum
    ISSN 1940-6029
    ISSN (online) 1940-6029
    DOI 10.1007/978-1-0716-1307-8_32
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Editorial: RNA modifications and epitranscriptomics, Volume II.

    Chen, Kunqi / Picardi, Ernesto / Han, Xiao / Nigita, Giovanni

    Frontiers in genetics

    2023  Volume 14, Page(s) 1229046

    Language English
    Publishing date 2023-06-07
    Publishing country Switzerland
    Document type Editorial
    ZDB-ID 2606823-0
    ISSN 1664-8021
    ISSN 1664-8021
    DOI 10.3389/fgene.2023.1229046
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Profiling RNA Editing in Single Cells.

    Fonzino, Adriano / Pesole, Graziano / Picardi, Ernesto

    Methods in molecular biology (Clifton, N.J.)

    2022  Volume 2584, Page(s) 347–370

    Abstract: RNA editing is a widespread molecular phenomenon occurring in a variety of organisms. In humans, it mainly involves the deamination of adenosine to inosine (A-to-I) in double-stranded RNAs by ADAR enzymes. A-to-I RNA editing has been investigated in ... ...

    Abstract RNA editing is a widespread molecular phenomenon occurring in a variety of organisms. In humans, it mainly involves the deamination of adenosine to inosine (A-to-I) in double-stranded RNAs by ADAR enzymes. A-to-I RNA editing has been investigated in different tissues as well as in diverse experimental and pathological conditions. By contrast, its biological role in single cells has not been explored in depth. Recent methodologies for cell sorting in combination with deep sequencing technologies have enabled the study of eukaryotic transcriptomes at single cell resolution, paving the way to the profiling of their epitranscriptomic dynamics.Here we describe a step-by-step protocol to detect and characterize A-to-I events occurring in publicly available single-cell RNAseq experiments from human alpha and beta pancreatic cells.
    MeSH term(s) Humans ; RNA Editing ; Adenosine Deaminase/genetics ; Inosine/genetics ; Inosine/metabolism ; Adenosine/genetics ; Adenosine/metabolism ; RNA, Double-Stranded ; RNA/genetics
    Chemical Substances Adenosine Deaminase (EC 3.5.4.4) ; Inosine (5A614L51CT) ; Adenosine (K72T3FS567) ; RNA, Double-Stranded ; RNA (63231-63-0)
    Language English
    Publishing date 2022-12-29
    Publishing country United States
    Document type Journal Article
    ISSN 1940-6029
    ISSN (online) 1940-6029
    DOI 10.1007/978-1-0716-2756-3_18
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Detection of ribonucleotides embedded in DNA by Nanopore sequencing.

    Grasso, Lavinia / Fonzino, Adriano / Manzari, Caterina / Leonardi, Tommaso / Picardi, Ernesto / Gissi, Carmela / Lazzaro, Federico / Pesole, Graziano / Muzi-Falconi, Marco

    Communications biology

    2024  Volume 7, Issue 1, Page(s) 491

    Abstract: Ribonucleotides represent the most common non-canonical nucleotides found in eukaryotic genomes. The sources of chromosome-embedded ribonucleotides and the mechanisms by which unrepaired rNMPs trigger genome instability and human pathologies are not ... ...

    Abstract Ribonucleotides represent the most common non-canonical nucleotides found in eukaryotic genomes. The sources of chromosome-embedded ribonucleotides and the mechanisms by which unrepaired rNMPs trigger genome instability and human pathologies are not fully understood. The available sequencing technologies only allow to indirectly deduce the genomic location of rNMPs. Oxford Nanopore Technologies (ONT) may overcome such limitation, revealing the sites of rNMPs incorporation in genomic DNA directly from raw sequencing signals. We synthesized two types of DNA molecules containing rNMPs at known or random positions and we developed data analysis pipelines for DNA-embedded ribonucleotides detection by ONT. We report that ONT can identify all four ribonucleotides incorporated in DNA by capturing rNMPs-specific alterations in nucleotide alignment features, current intensity, and dwell time. We propose that ONT may be successfully employed to directly map rNMPs in genomic DNA and we suggest a strategy to build an ad hoc basecaller to analyse native genomes.
    MeSH term(s) Nanopore Sequencing/methods ; Ribonucleotides/genetics ; DNA/genetics ; Humans ; Sequence Analysis, DNA/methods ; Nanopores
    Chemical Substances Ribonucleotides ; DNA (9007-49-2)
    Language English
    Publishing date 2024-04-23
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 2399-3642
    ISSN (online) 2399-3642
    DOI 10.1038/s42003-024-06077-w
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Mitochondrial and Nuclear DNA Variants in Amyotrophic Lateral Sclerosis: Enrichment in the Mitochondrial Control Region and Sirtuin Pathway Genes in Spinal Cord Tissue.

    Cox, Sharon Natasha / Lo Giudice, Claudio / Lavecchia, Anna / Poeta, Maria Luana / Chiara, Matteo / Picardi, Ernesto / Pesole, Graziano

    Biomolecules

    2024  Volume 14, Issue 4

    Abstract: Amyotrophic Lateral Sclerosis (ALS) is a progressive disease with prevalent mitochondrial dysfunctions affecting both upper and lower motor neurons in the motor cortex, brainstem, and spinal cord. Despite mitochondria having their own genome (mtDNA), in ... ...

    Abstract Amyotrophic Lateral Sclerosis (ALS) is a progressive disease with prevalent mitochondrial dysfunctions affecting both upper and lower motor neurons in the motor cortex, brainstem, and spinal cord. Despite mitochondria having their own genome (mtDNA), in humans, most mitochondrial genes are encoded by the nuclear genome (nDNA). Our study aimed to simultaneously screen for nDNA and mtDNA genomes to assess for specific variant enrichment in ALS compared to control tissues. Here, we analysed whole exome (WES) and whole genome (WGS) sequencing data from spinal cord tissues, respectively, of 6 and 12 human donors. A total of 31,257 and 301,241 variants in nuclear-encoded mitochondrial genes were identified from WES and WGS, respectively, while mtDNA reads accounted for 73 and 332 variants. Despite technical differences, both datasets consistently revealed a specific enrichment of variants in the mitochondrial Control Region (CR) and in several of these genes directly associated with mitochondrial dynamics or with Sirtuin pathway genes within ALS tissues. Overall, our data support the hypothesis of a variant burden in specific genes, highlighting potential actionable targets for therapeutic interventions in ALS.
    MeSH term(s) Amyotrophic Lateral Sclerosis/genetics ; Amyotrophic Lateral Sclerosis/metabolism ; Humans ; Spinal Cord/metabolism ; Spinal Cord/pathology ; DNA, Mitochondrial/genetics ; Sirtuins/genetics ; Sirtuins/metabolism ; Male ; Female ; Middle Aged ; Mitochondria/genetics ; Mitochondria/metabolism ; Cell Nucleus/genetics ; Cell Nucleus/metabolism ; Aged ; Exome Sequencing
    Chemical Substances DNA, Mitochondrial ; Sirtuins (EC 3.5.1.-)
    Language English
    Publishing date 2024-03-28
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2701262-1
    ISSN 2218-273X ; 2218-273X
    ISSN (online) 2218-273X
    ISSN 2218-273X
    DOI 10.3390/biom14040411
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Macroalgal microbiomes unveil a valuable genetic resource for halogen metabolism.

    Lavecchia, Anna / Fosso, Bruno / Engelen, Aschwin H / Borin, Sara / Manzari, Caterina / Picardi, Ernesto / Pesole, Graziano / Placido, Antonio

    Microbiome

    2024  Volume 12, Issue 1, Page(s) 47

    Abstract: Background: Macroalgae, especially reds (Rhodophyta Division) and browns (Phaeophyta Division), are known for producing various halogenated compounds. Yet, the reasons underlying their production and the fate of these metabolites remain largely unknown. ...

    Abstract Background: Macroalgae, especially reds (Rhodophyta Division) and browns (Phaeophyta Division), are known for producing various halogenated compounds. Yet, the reasons underlying their production and the fate of these metabolites remain largely unknown. Some theories suggest their potential antimicrobial activity and involvement in interactions between macroalgae and prokaryotes. However, detailed investigations are currently missing on how the genetic information of prokaryotic communities associated with macroalgae may influence the fate of organohalogenated molecules.
    Results: To address this challenge, we created a specialized dataset containing 161 enzymes, each with a complete enzyme commission number, known to be involved in halogen metabolism. This dataset served as a reference to annotate the corresponding genes encoded in both the metagenomic contigs and 98 metagenome-assembled genomes (MAGs) obtained from the microbiome of 2 red (Sphaerococcus coronopifolius and Asparagopsis taxiformis) and 1 brown (Halopteris scoparia) macroalgae. We detected many dehalogenation-related genes, particularly those with hydrolytic functions, suggesting their potential involvement in the degradation of a wide spectrum of halocarbons and haloaromatic molecules, including anthropogenic compounds. We uncovered an array of degradative gene functions within MAGs, spanning various bacterial orders such as Rhodobacterales, Rhizobiales, Caulobacterales, Geminicoccales, Sphingomonadales, Granulosicoccales, Microtrichales, and Pseudomonadales. Less abundant than degradative functions, we also uncovered genes associated with the biosynthesis of halogenated antimicrobial compounds and metabolites.
    Conclusion: The functional data provided here contribute to understanding the still largely unexplored role of unknown prokaryotes. These findings support the hypothesis that macroalgae function as holobionts, where the metabolism of halogenated compounds might play a role in symbiogenesis and act as a possible defense mechanism against environmental chemical stressors. Furthermore, bacterial groups, previously never connected with organohalogen metabolism, e.g., Caulobacterales, Geminicoccales, Granulosicoccales, and Microtrichales, functionally characterized through MAGs reconstruction, revealed a biotechnologically relevant gene content, useful in synthetic biology, and bioprospecting applications. Video Abstract.
    MeSH term(s) Rhodophyta/genetics ; Rhodophyta/metabolism ; Microbiota/genetics ; Bacteria/genetics ; Bacteria/metabolism ; Seaweed/genetics ; Seaweed/metabolism ; Metagenome ; Anti-Infective Agents ; Halogens/metabolism
    Chemical Substances Anti-Infective Agents ; Halogens
    Language English
    Publishing date 2024-03-07
    Publishing country England
    Document type Video-Audio Media ; Journal Article
    ZDB-ID 2697425-3
    ISSN 2049-2618 ; 2049-2618
    ISSN (online) 2049-2618
    ISSN 2049-2618
    DOI 10.1186/s40168-023-01740-6
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Detection of A-to-I RNA Editing in SARS-COV-2.

    Picardi, Ernesto / Mansi, Luigi / Pesole, Graziano

    Genes

    2021  Volume 13, Issue 1

    Abstract: ADAR1-mediated deamination of adenosines in long double-stranded RNAs plays an important role in modulating the innate immune response. However, recent investigations based on metatranscriptomic samples of COVID-19 patients and SARS-COV-2-infected Vero ... ...

    Abstract ADAR1-mediated deamination of adenosines in long double-stranded RNAs plays an important role in modulating the innate immune response. However, recent investigations based on metatranscriptomic samples of COVID-19 patients and SARS-COV-2-infected Vero cells have recovered contrasting findings. Using RNAseq data from time course experiments of infected human cell lines and transcriptome data from Vero cells and clinical samples, we prove that A-to-G changes observed in SARS-COV-2 genomes represent genuine RNA editing events, likely mediated by ADAR1. While the A-to-I editing rate is generally low, changes are distributed along the entire viral genome, are overrepresented in exonic regions, and are (in the majority of cases) nonsynonymous. The impact of RNA editing on virus-host interactions could be relevant to identify potential targets for therapeutic interventions.
    MeSH term(s) Adenosine/metabolism ; Adenosine Deaminase/genetics ; Adenosine Deaminase/immunology ; Animals ; COVID-19/genetics ; COVID-19/metabolism ; COVID-19/virology ; Cell Line, Tumor ; Chlorocebus aethiops ; DEAD Box Protein 58/genetics ; DEAD Box Protein 58/immunology ; Deamination ; Epithelial Cells/immunology ; Epithelial Cells/virology ; Genome, Viral ; Host-Pathogen Interactions/genetics ; Host-Pathogen Interactions/immunology ; Humans ; Immunity, Innate ; Inosine/metabolism ; Interferon-Induced Helicase, IFIH1/genetics ; Interferon-Induced Helicase, IFIH1/immunology ; Interferon-beta/genetics ; Interferon-beta/immunology ; RNA Editing ; RNA, Double-Stranded/genetics ; RNA, Double-Stranded/immunology ; RNA, Viral/genetics ; RNA, Viral/immunology ; RNA-Binding Proteins/genetics ; RNA-Binding Proteins/immunology ; Receptors, Immunologic/genetics ; Receptors, Immunologic/immunology ; SARS-CoV-2/genetics ; SARS-CoV-2/metabolism ; SARS-CoV-2/pathogenicity ; Transcriptome ; Vero Cells
    Chemical Substances RNA, Double-Stranded ; RNA, Viral ; RNA-Binding Proteins ; Receptors, Immunologic ; Inosine (5A614L51CT) ; Interferon-beta (77238-31-4) ; ADAR protein, human (EC 3.5.4.37) ; Adenosine Deaminase (EC 3.5.4.4) ; RIGI protein, human (EC 3.6.1.-) ; IFIH1 protein, human (EC 3.6.1.-) ; DEAD Box Protein 58 (EC 3.6.4.13) ; Interferon-Induced Helicase, IFIH1 (EC 3.6.4.13) ; Adenosine (K72T3FS567)
    Language English
    Publishing date 2021-12-23
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2527218-4
    ISSN 2073-4425 ; 2073-4425
    ISSN (online) 2073-4425
    ISSN 2073-4425
    DOI 10.3390/genes13010041
    Database MEDical Literature Analysis and Retrieval System OnLINE

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