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Searching for transposable elements in hematological malignancies

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F65269705%3A_____%2F19%3A00072426" target="_blank" >RIV/65269705:_____/19:00072426 - isvavai.cz</a>

  • Výsledek na webu

    <a href="http://phdretreat.ceitec.cz/joint-retreat-2019/" target="_blank" >http://phdretreat.ceitec.cz/joint-retreat-2019/</a>

  • DOI - Digital Object Identifier

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Searching for transposable elements in hematological malignancies

  • Popis výsledku v původním jazyce

    Transposable elements, or transposons, are DNA units present in eukaryotic organisms in a broad diversity of their structures. They have played an important role in evolution of many genomes. In the human genome, the vast majority of transposons is represented by retroelements (REs) that can integrate new copies through RNA-mediated mechanisms. The long interspersed nucleic elements (LINE-1 or L1) utilize a &quot;copy-and-paste&quot; mechanism to retrotranspose copies into new genomic loci. Active L1 retrotransposons also drive retrotransposition of other mobile DNAs, namely, Alu, short interspersed elements (SINEs), and SVA transposons. Recent findings imply that genomic instability of cancer is associated with transposon reactivation. The main goal of our research is to explore RE activity in different types of hematological malignancies. To identify tumor-specific RE insertions, we adopted a protocol based on high-throughput sequencing of amplicons containing a part of AluYa5, Alu-Ya8 or L1-HS insertions, and their adjacent genomic regions. By using unique molecular identifiers, we aim to estimate the percentage of cancer cells bearing each particular insertion. We performed a pilot experiment on 42 tumornormal sample pairs from patients with chronic lymphocytic leukemia, acute lymphoblastic leukemia, and myelodysplastic syndrome. The libraries were sequenced on Illumina NextSeq and obtained sequences are currently subjected to an in-house bioinformatics pipeline for identification of somatic RE insertions.

  • Název v anglickém jazyce

    Searching for transposable elements in hematological malignancies

  • Popis výsledku anglicky

    Transposable elements, or transposons, are DNA units present in eukaryotic organisms in a broad diversity of their structures. They have played an important role in evolution of many genomes. In the human genome, the vast majority of transposons is represented by retroelements (REs) that can integrate new copies through RNA-mediated mechanisms. The long interspersed nucleic elements (LINE-1 or L1) utilize a &quot;copy-and-paste&quot; mechanism to retrotranspose copies into new genomic loci. Active L1 retrotransposons also drive retrotransposition of other mobile DNAs, namely, Alu, short interspersed elements (SINEs), and SVA transposons. Recent findings imply that genomic instability of cancer is associated with transposon reactivation. The main goal of our research is to explore RE activity in different types of hematological malignancies. To identify tumor-specific RE insertions, we adopted a protocol based on high-throughput sequencing of amplicons containing a part of AluYa5, Alu-Ya8 or L1-HS insertions, and their adjacent genomic regions. By using unique molecular identifiers, we aim to estimate the percentage of cancer cells bearing each particular insertion. We performed a pilot experiment on 42 tumornormal sample pairs from patients with chronic lymphocytic leukemia, acute lymphoblastic leukemia, and myelodysplastic syndrome. The libraries were sequenced on Illumina NextSeq and obtained sequences are currently subjected to an in-house bioinformatics pipeline for identification of somatic RE insertions.

Klasifikace

  • Druh

    O - Ostatní výsledky

  • CEP obor

  • OECD FORD obor

    30205 - Hematology

Návaznosti výsledku

  • Projekt

    <a href="/cs/project/GA19-11299S" target="_blank" >GA19-11299S: Úloha transpozibilních elementů u hematologických malignit</a><br>

  • Návaznosti

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Ostatní

  • Rok uplatnění

    2019

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů