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Searching for transposable elements in hematological malignancies

The result's identifiers

  • Result code in 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>

  • Result on the web

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

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Searching for transposable elements in hematological malignancies

  • Original language description

    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.

  • Czech name

  • Czech description

Classification

  • Type

    O - Miscellaneous

  • CEP classification

  • OECD FORD branch

    30205 - Hematology

Result continuities

  • Project

    <a href="/en/project/GA19-11299S" target="_blank" >GA19-11299S: The role of transposable element activity in hematological malignacies</a><br>

  • Continuities

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

Others

  • Publication year

    2019

  • Confidentiality

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