LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 8 of total 8

Search options

  1. Article ; Online: PRMT5 regulates ATF4 transcript splicing and oxidative stress response

    Magdalena M. Szewczyk / Genna M. Luciani / Victoria Vu / Alex Murison / David Dilworth / Samir H. Barghout / Mathieu Lupien / Cheryl H. Arrowsmith / Mark D. Minden / Dalia Barsyte-Lovejoy

    Redox Biology, Vol 51, Iss , Pp 102282- (2022)

    2022  

    Abstract: Protein methyltransferase 5 (PRMT5) symmetrically dimethylates arginine residues leading to regulation of transcription and splicing programs. Although PRMT5 has emerged as an attractive oncology target, the molecular determinants of PRMT5 dependency in ... ...

    Abstract Protein methyltransferase 5 (PRMT5) symmetrically dimethylates arginine residues leading to regulation of transcription and splicing programs. Although PRMT5 has emerged as an attractive oncology target, the molecular determinants of PRMT5 dependency in cancer remain incompletely understood. Our transcriptomic analysis identified PRMT5 regulation of the activating transcription factor 4 (ATF4) pathway in acute myelogenous leukemia (AML). PRMT5 inhibition resulted in the expression of unstable, intron-retaining ATF4 mRNA that is detained in the nucleus. Concurrently, the decrease in the spliced cytoplasmic transcript of ATF4 led to lower levels of ATF4 protein and downregulation of ATF4 target genes. Upon loss of functional PRMT5, cells with low ATF4 displayed increased oxidative stress, growth arrest, and cellular senescence. Interestingly, leukemia cells with EVI1 oncogene overexpression demonstrated dependence on PRMT5 function. EVI1 and ATF4 regulated gene signatures were inversely correlated. We show that EVI1-high AML cells have reduced ATF4 levels, elevated baseline reactive oxygen species and increased sensitivity to PRMT5 inhibition. Thus, EVI1-high cells demonstrate dependence on PRMT5 function and regulation of oxidative stress response. Overall, our findings identify the PRMT5-ATF4 axis to be safeguarding the cellular redox balance that is especially important in high oxidative stress states, such as those that occur with EVI1 overexpression.
    Keywords Epigenetics ; PRMT5 ; Oxidative stress ; Splicing ; Intron retention ; ATF4 ; Medicine (General) ; R5-920 ; Biology (General) ; QH301-705.5
    Language English
    Publishing date 2022-05-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  2. Article ; Online: The novel nematicide wact-86 interacts with aldicarb to kill nematodes.

    Andrew R Burns / Rachel Bagg / May Yeo / Genna M Luciani / Michael Schertzberg / Andy G Fraser / Peter J Roy

    PLoS Neglected Tropical Diseases, Vol 11, Iss 4, p e

    2017  Volume 0005502

    Abstract: Parasitic nematodes negatively impact human and animal health worldwide. The market withdrawal of nematicidal agents due to unfavourable toxicities has limited the available treatment options. In principle, co-administering nematicides at lower doses ... ...

    Abstract Parasitic nematodes negatively impact human and animal health worldwide. The market withdrawal of nematicidal agents due to unfavourable toxicities has limited the available treatment options. In principle, co-administering nematicides at lower doses along with molecules that potentiate their activity could mitigate adverse toxicities without compromising efficacy. Here, we screened for new small molecules that interact with aldicarb, which is a highly effective treatment for plant-parasitic nematodes whose toxicity hampers its utility. From our collection of 638 worm-bioactive compounds, we identified 20 molecules that interact positively with aldicarb to either kill or arrest the growth of the model nematode Caenorhabditis elegans. We investigated the mechanism of interaction between aldicarb and one of these novel nematicides called wact-86. We found that the carboxylesterase enzyme GES-1 hydrolyzes wact-86, and that the interaction is manifested by aldicarb's inhibition of wact-86's metabolism by GES-1. This work demonstrates the utility of C. elegans as a platform to search for new molecules that can positively interact with industrial nematicides, and provides proof-of-concept for prospective discovery efforts.
    Keywords Arctic medicine. Tropical medicine ; RC955-962 ; Public aspects of medicine ; RA1-1270
    Language English
    Publishing date 2017-04-01T00:00:00Z
    Publisher Public Library of Science (PLoS)
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  3. Article ; Online: Author Correction

    Andrew R. Burns / Genna M. Luciani / Gabriel Musso / Rachel Bagg / May Yeo / Yuqian Zhang / Luckshi Rajendran / John Glavin / Robert Hunter / Elizabeth Redman / Susan Stasiuk / Michael Schertzberg / G. Angus McQuibban / Conor R. Caffrey / Sean R. Cutler / Mike Tyers / Guri Giaever / Corey Nislow / Andy G. Fraser /
    Calum A. MacRae / John Gilleard / Peter J. Roy

    Nature Communications, Vol 11, Iss 1, Pp 1-

    Caenorhabditis elegans is a useful model for anthelmintic discovery

    2020  Volume 1

    Abstract: An amendment to this paper has been published and can be accessed via a link at the top of the paper. ...

    Abstract An amendment to this paper has been published and can be accessed via a link at the top of the paper.
    Keywords Science ; Q
    Language English
    Publishing date 2020-07-01T00:00:00Z
    Publisher Nature Publishing Group
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  4. Article ; Online: Author Correction

    Andrew R. Burns / Genna M. Luciani / Gabriel Musso / Rachel Bagg / May Yeo / Yuqian Zhang / Luckshi Rajendran / John Glavin / Robert Hunter / Elizabeth Redman / Susan Stasiuk / Michael Schertzberg / G. Angus McQuibban / Conor R. Caffrey / Sean R. Cutler / Mike Tyers / Guri Giaever / Corey Nislow / Andy G. Fraser /
    Calum A. MacRae / John Gilleard / Peter J. Roy

    Nature Communications, Vol 11, Iss 1, Pp 1-

    Caenorhabditis elegans is a useful model for anthelmintic discovery

    2020  Volume 1

    Abstract: An amendment to this paper has been published and can be accessed via a link at the top of the paper. ...

    Abstract An amendment to this paper has been published and can be accessed via a link at the top of the paper.
    Keywords Science ; Q
    Language English
    Publishing date 2020-07-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  5. Article ; Online: Targeting bivalency de-represses Indian Hedgehog and inhibits self-renewal of colorectal cancer-initiating cells

    Evelyne Lima-Fernandes / Alex Murison / Tiago da Silva Medina / Yadong Wang / Anqi Ma / Cherry Leung / Genna M. Luciani / Jennifer Haynes / Aaron Pollett / Constanze Zeller / Shili Duan / Antonija Kreso / Dalia Barsyte-Lovejoy / Bradly G. Wouters / Jian Jin / Daniel D. De Carvalho / Mathieu Lupien / Cheryl H. Arrowsmith / Catherine A. O’Brien

    Nature Communications, Vol 10, Iss 1, Pp 1-

    2019  Volume 14

    Abstract: The presence of bivalent epigenetic active and repressive histone marks control lineage-specific differentiation in embryonic stem cells. Here, the authors reveal that bivalent marks repress the differentiation gene IHH in colorectal cancer-initiating ... ...

    Abstract The presence of bivalent epigenetic active and repressive histone marks control lineage-specific differentiation in embryonic stem cells. Here, the authors reveal that bivalent marks repress the differentiation gene IHH in colorectal cancer-initiating cells, and can be targeted by EZH2 inhibition
    Keywords Science ; Q
    Language English
    Publishing date 2019-03-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  6. Article ; Online: Targeting bivalency de-represses Indian Hedgehog and inhibits self-renewal of colorectal cancer-initiating cells

    Evelyne Lima-Fernandes / Alex Murison / Tiago da Silva Medina / Yadong Wang / Anqi Ma / Cherry Leung / Genna M. Luciani / Jennifer Haynes / Aaron Pollett / Constanze Zeller / Shili Duan / Antonija Kreso / Dalia Barsyte-Lovejoy / Bradly G. Wouters / Jian Jin / Daniel D. De Carvalho / Mathieu Lupien / Cheryl H. Arrowsmith / Catherine A. O’Brien

    Nature Communications, Vol 10, Iss 1, Pp 1-

    2019  Volume 14

    Abstract: The presence of bivalent epigenetic active and repressive histone marks control lineage-specific differentiation in embryonic stem cells. Here, the authors reveal that bivalent marks repress the differentiation gene IHH in colorectal cancer-initiating ... ...

    Abstract The presence of bivalent epigenetic active and repressive histone marks control lineage-specific differentiation in embryonic stem cells. Here, the authors reveal that bivalent marks repress the differentiation gene IHH in colorectal cancer-initiating cells, and can be targeted by EZH2 inhibition
    Keywords Science ; Q
    Language English
    Publishing date 2019-03-01T00:00:00Z
    Publisher Nature Publishing Group
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  7. Article ; Online: Discovery of a chemical probe for PRDM9

    Abdellah Allali-Hassani / Magdalena M. Szewczyk / Danton Ivanochko / Shawna L. Organ / Jabez Bok / Jessica Sook Yuin Ho / Florence P. H. Gay / Fengling Li / Levi Blazer / Mohammad S. Eram / Levon Halabelian / David Dilworth / Genna M. Luciani / Evelyne Lima-Fernandes / Qin Wu / Peter Loppnau / Nathan Palmer / S. Zakiah A. Talib / Peter J. Brown /
    Matthieu Schapira / Philipp Kaldis / Ronan C. O’Hagan / Ernesto Guccione / Dalia Barsyte-Lovejoy / Cheryl H. Arrowsmith / John M. Sanders / Solomon D. Kattar / D. Jonathan Bennett / Benjamin Nicholson / Masoud Vedadi

    Nature Communications, Vol 10, Iss 1, Pp 1-

    2019  Volume 11

    Abstract: PRDM9 is a PR domain containing histone methyl transferase which expression is normally restricted to the germline that has also been linked to a number of somatic cancers. Here the authors describe the identification of a small molecule that selectivity ...

    Abstract PRDM9 is a PR domain containing histone methyl transferase which expression is normally restricted to the germline that has also been linked to a number of somatic cancers. Here the authors describe the identification of a small molecule that selectivity inhibits the methyltransferase activity of PRDM9 in biochemical and cellular assays
    Keywords Science ; Q
    Language English
    Publishing date 2019-12-01T00:00:00Z
    Publisher Nature Publishing Group
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  8. Article ; Online: Discovery of a chemical probe for PRDM9

    Abdellah Allali-Hassani / Magdalena M. Szewczyk / Danton Ivanochko / Shawna L. Organ / Jabez Bok / Jessica Sook Yuin Ho / Florence P. H. Gay / Fengling Li / Levi Blazer / Mohammad S. Eram / Levon Halabelian / David Dilworth / Genna M. Luciani / Evelyne Lima-Fernandes / Qin Wu / Peter Loppnau / Nathan Palmer / S. Zakiah A. Talib / Peter J. Brown /
    Matthieu Schapira / Philipp Kaldis / Ronan C. O’Hagan / Ernesto Guccione / Dalia Barsyte-Lovejoy / Cheryl H. Arrowsmith / John M. Sanders / Solomon D. Kattar / D. Jonathan Bennett / Benjamin Nicholson / Masoud Vedadi

    Nature Communications, Vol 10, Iss 1, Pp 1-

    2019  Volume 11

    Abstract: PRDM9 is a PR domain containing histone methyl transferase which expression is normally restricted to the germline that has also been linked to a number of somatic cancers. Here the authors describe the identification of a small molecule that selectivity ...

    Abstract PRDM9 is a PR domain containing histone methyl transferase which expression is normally restricted to the germline that has also been linked to a number of somatic cancers. Here the authors describe the identification of a small molecule that selectivity inhibits the methyltransferase activity of PRDM9 in biochemical and cellular assays
    Keywords Science ; Q
    Language English
    Publishing date 2019-12-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

To top