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      KSHV 3.0: A State-of-the-Art Annotation of the Kaposi’s Sarcoma-Associated Herpesvirus Transcriptome Using Cross-Platform Sequencing

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          Abstract

          Kaposi’s sarcoma-associated herpesvirus (KSHV) is a large, oncogenic DNA virus belonging to the gammaherpesvirus subfamily. KSHV has been extensively studied with various high-throughput RNA-sequencing approaches to map the transcription start and end sites, the splice junctions, and the translation initiation sites. Despite these efforts, the comprehensive annotation of the viral transcriptome remains incomplete. In the present study, we generated a long-read sequencing dataset of the lytic and latent KSHV transcriptome using native RNA and direct cDNA sequencing methods. This was supplemented with CAGE sequencing based on a short-read platform. We also utilized datasets from previous publications for our analysis. As a result of this combined approach, we have identified a number of novel viral transcripts and RNA isoforms and have either corroborated or improved the annotation of previously identified viral RNA molecules, thereby notably enhancing our comprehension of the transcriptomic architecture of the KSHV genome. We also evaluated the coding capability of transcripts previously thought to be non-coding, by integrating our data on the viral transcripts with translatomic information from other publications.

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          Most cited references80

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          Identification of herpesvirus-like DNA sequences in AIDS-associated Kaposi's sarcoma.

          Representational difference analysis was used to isolate unique sequences present in more than 90 percent of Kaposi's sarcoma (KS) tissues obtained from patients with acquired immunodeficiency syndrome (AIDS). These sequences were not present in tissue DNA from non-AIDS patients, but were present in 15 percent of non-KS tissue DNA samples from AIDS patients. The sequences are homologous to, but distinct from, capsid and tegument protein genes of the Gammaherpesvirinae, herpesvirus saimiri and Epstein-Barr virus. These KS-associated herpesvirus-like (KSHV) sequences appear to define a new human herpesvirus.
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            Efficient persistence of extrachromosomal KSHV DNA mediated by latency-associated nuclear antigen.

            Primary effusion lymphoma (PEL) cells harbor Kaposi's sarcoma-associated herpesvirus (KSHV) episomes and express a KSHV-encoded latency-associated nuclear antigen (LANA). In PEL cells, LANA and KSHV DNA colocalized in dots in interphase nuclei and along mitotic chromosomes. In the absence of KSHV DNA, LANA was diffusely distributed in the nucleus or on mitotic chromosomes. In lymphoblasts, LANA was necessary and sufficient for the persistence of episomes containing a specific KSHV DNA fragment. Furthermore, LANA colocalized with the artificial KSHV DNA episomes in nuclei and along mitotic chromosomes. These results support a model in which LANA tethers KSHV DNA to chromosomes during mitosis to enable the efficient segregation of KSHV episomes to progeny cells.
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              KSHV and the pathogenesis of Kaposi sarcoma: listening to human biology and medicine.

              Don Ganem (2010)
              The linkage of Kaposi sarcoma (KS) to infection by a novel human herpesvirus (Kaposi sarcoma-associated herpesvirus [KSHV]) is one of the great successes of contemporary biomedical research and was achieved by using advanced genomic technologies in a manner informed by a nuanced understanding of epidemiology and clinical investigation. Ongoing efforts to understand the molecular mechanisms by which KSHV infection predisposes to KS continue to be powerfully influenced by insights emanating from the clinic. Here, recent developments in KS pathogenesis are reviewed, with particular emphasis on clinical, pathologic, and molecular observations that highlight the many differences between this process and tumorigenesis by other oncogenic viruses.
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                Author and article information

                Journal
                bioRxiv
                BIORXIV
                bioRxiv
                Cold Spring Harbor Laboratory
                21 September 2023
                : 2023.09.21.558842
                Affiliations
                [1 ]Department of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary
                [2 ]Department of Oral Biology, University of Florida College of Dentistry, Gainesville, Florida, USA
                Author notes
                [#]

                The first three authors contributed equally to this work

                [*]

                Shared senior/corresponding authors

                Author contributions

                ÁD: Participated in RNA purification and long-read sequencing

                ÁF: Contributed to bioinformatics and data interpretation

                BK: Contributed to bioinformatics, data interpretation and visualization

                DT: Performed library preparation, long-read and CAGE sequencing, participated in data interpretation, and drafted the manuscript

                GG: Contributed to sequencing and bioinformatics

                GT: Conducted bioinformatics, data, interpretation, and integration of data

                IP: Participated in data analysis integration, visualization and drafted the manuscript

                LMS: Participated in cell propagation and carried out RNA purification

                ZB: Conceived and designed the experiments, supervised the study, and wrote the manuscript

                ZT: Contributed to the experiment design and drafted the manuscript

                All authors read and approved the final paper.

                Article
                10.1101/2023.09.21.558842
                10542539
                37790386
                0e2f33c6-649d-4aa2-9c6a-afec164257ad

                This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.

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                kaposi’s sarcoma-associated herpesvirus (kshv),herpesviruses,transcriptome,nanopore sequencing,cage,tss,tes,tis

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