LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 10 of total 34

Search options

  1. Article ; Online: Direct and Base Excision Repair-Mediated Regulation of a GC-Rich cis -Element in Response to 5-Formylcytosine and 5-Carboxycytosine

    Nadine Müller / Eveliina Ponkkonen / Thomas Carell / Andriy Khobta

    International Journal of Molecular Sciences, Vol 22, Iss 11025, p

    2021  Volume 11025

    Abstract: Stepwise oxidation of the epigenetic mark 5-methylcytosine and base excision repair (BER) of the resulting 5-formylcytosine (5-fC) and 5-carboxycytosine (5-caC) may provide a mechanism for reactivation of epigenetically silenced genes; however, the ... ...

    Abstract Stepwise oxidation of the epigenetic mark 5-methylcytosine and base excision repair (BER) of the resulting 5-formylcytosine (5-fC) and 5-carboxycytosine (5-caC) may provide a mechanism for reactivation of epigenetically silenced genes; however, the functions of 5-fC and 5-caC at defined gene elements are scarcely explored. We analyzed the expression of reporter constructs containing either 2′-deoxy-(5-fC/5-caC) or their BER-resistant 2′-fluorinated analogs, asymmetrically incorporated into CG-dinucleotide of the GC box cis -element (5′-TGGGCGGAGC) upstream from the RNA polymerase II core promoter. In the absence of BER, 5-caC caused a strong inhibition of the promoter activity, whereas 5-fC had almost no effect, similar to 5-methylcytosine or 5-hydroxymethylcytosine. BER of 5-caC caused a transient but significant promoter reactivation, succeeded by silencing during the following hours. Both responses strictly required thymine DNA glycosylase (TDG); however, the silencing phase additionally demanded a 5′-endonuclease (likely APE1) activity and was also induced by 5-fC or an apurinic/apyrimidinic site. We propose that 5-caC may act as a repressory mark to prevent premature activation of promoters undergoing the final stages of DNA demethylation, when the symmetric CpG methylation has already been lost. Remarkably, the downstream promoter activation or repression responses are regulated by two separate BER steps, where TDG and APE1 act as potential switches.
    Keywords DNA demethylation ; 5-formylcytosine ; 5-carboxycytosine ; thymine DNA glycosylase (TDG) ; base excision repair (BER) ; gene regulation ; Biology (General) ; QH301-705.5 ; Chemistry ; QD1-999
    Subject code 572
    Language English
    Publishing date 2021-10-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  2. Article ; Online: Rethinking the tools of the RNA world

    Antony Crisp / Thomas Carell

    eLife, Vol

    2018  Volume 7

    Abstract: An artificially evolved ribozyme can catalyse the synthesis of RNA by using trinucleotide triphosphates as building blocks. ...

    Abstract An artificially evolved ribozyme can catalyse the synthesis of RNA by using trinucleotide triphosphates as building blocks.
    Keywords ribozyme ; RNA ; origins of life ; molecular evolution ; ribosome ; triplets ; Medicine ; R ; Science ; Q ; Biology (General) ; QH301-705.5
    Language English
    Publishing date 2018-06-01T00:00:00Z
    Publisher eLife Sciences Publications Ltd
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  3. Article ; Online: A Unifying Concept for the Prebiotic Formation of RNA Pyrimidine Nucleosides

    Jonas Feldmann / Mads K. Skaanning / Marcus Lommel / Tobias Kernmayr / Dr. Peter Mayer / Prof. Dr. Thomas Carell

    ChemistryEurope, Vol 1, Iss 1, Pp n/a-n/a (2023)

    2023  

    Abstract: Abstract The question of how nucleosides might have formed as essential precursor molecules on the early Earth is one of the many challenges associated with the origin of life. In this context, the prebiotic synthesis of pyrimidine nucleosides is ... ...

    Abstract Abstract The question of how nucleosides might have formed as essential precursor molecules on the early Earth is one of the many challenges associated with the origin of life. In this context, the prebiotic synthesis of pyrimidine nucleosides is controversially discussed. For the pyrimidines, two at first glance contradictory prebiotically plausible reaction pathways have been proposed, based on either oxazole or isoxazole chemistry. This study shows that these two reaction sequences can be merged under prebiotically reasonable conditions, suggesting that both pathways could have co‐existed and possibly interacted. The key precursor 3‐aminoisoxazole was found to react with the key intermediate of the oxazole route (ribo‐2‐(methylthio)oxazoline), to form a ribo‐isoxazole‐oxazoline hybrid structure, which collapses upon reductive N−O bond cleavage to give the nucleoside cytidine. The data suggest that different, interacting prebiotically plausible chemical pathways may have created the key molecules of life on the early Earth.
    Keywords 3-aminoisoxazole ; copper catalysis ; origin of life ; prebiotic chemistry ; pyrimidine nucleosides ; Chemistry ; QD1-999
    Subject code 540
    Language English
    Publishing date 2023-07-01T00:00:00Z
    Publisher Wiley-VCH
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  4. Article ; Online: Publisher Correction

    Sidney Becker / Christina Schneider / Antony Crisp / Thomas Carell

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

    Non-canonical nucleosides and chemistry of the emergence of life

    2019  Volume 1

    Abstract: The original version of this Article contained errors in the citations in the second, third and fourth sentences of the first paragraph of the ‘Life and LUCA’ section, which incorrectly read ‘Its development is explained by Darwinian evolution, which ... ...

    Abstract The original version of this Article contained errors in the citations in the second, third and fourth sentences of the first paragraph of the ‘Life and LUCA’ section, which incorrectly read ‘Its development is explained by Darwinian evolution, which must have begun with rudimentary “living” vesicles that at some point transitioned into what we call the last universal common ancestor (LUCA)2. LUCA is a hypothetical life form obtained from phylogenetic analysis from which all three kingdoms of life originated3. To our understanding, LUCA already possessed the capacity to synthesize specific building blocks such as amino acids, nucleotides and lipids2.’ The correct version states ‘(LUCA)1’ in place of ‘(LUCA)2’, ‘originated2’ instead of ‘originated3’ and ‘lipids1’ rather than ‘lipids2’. This has been corrected in both the PDF and HTML versions of the Article.
    Keywords Science ; Q
    Language English
    Publishing date 2019-01-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  5. Article ; Online: Synthesis and structure elucidation of the human tRNA nucleoside mannosyl-queuosine

    Markus Hillmeier / Mirko Wagner / Timm Ensfelder / Eva Korytiakova / Peter Thumbs / Markus Müller / Thomas Carell

    Nature Communications, Vol 12, Iss 1, Pp 1-

    2021  Volume 9

    Abstract: Mannosyl-queuosine (manQ) is a non-canonical RNA nucleoside present in the anticodon loop of certain tRNAs. Here, the authors use a combination of total synthesis and mass spectrometry to contradict the literature-reported structure and show that manQ ... ...

    Abstract Mannosyl-queuosine (manQ) is a non-canonical RNA nucleoside present in the anticodon loop of certain tRNAs. Here, the authors use a combination of total synthesis and mass spectrometry to contradict the literature-reported structure and show that manQ features an alpha-allyl connectivity of its mannose moiety.
    Keywords Science ; Q
    Language English
    Publishing date 2021-12-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  6. Article ; Online: Non-canonical nucleosides and chemistry of the emergence of life

    Sidney Becker / Christina Schneider / Antony Crisp / Thomas Carell

    Nature Communications, Vol 9, Iss 1, Pp 1-

    2018  Volume 4

    Abstract: Abstract Prebiotic chemistry, driven by changing environmental parameters provides canonical and a multitude of non-canonical nucleosides. This suggests that Watson-Crick base pairs were selected from a diverse pool of nucleosides in a pre-Darwinian ... ...

    Abstract Abstract Prebiotic chemistry, driven by changing environmental parameters provides canonical and a multitude of non-canonical nucleosides. This suggests that Watson-Crick base pairs were selected from a diverse pool of nucleosides in a pre-Darwinian chemical evolution process.
    Keywords Science ; Q
    Language English
    Publishing date 2018-12-01T00:00:00Z
    Publisher Nature Publishing Group
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  7. Article ; Online: Non-canonical nucleosides and chemistry of the emergence of life

    Sidney Becker / Christina Schneider / Antony Crisp / Thomas Carell

    Nature Communications, Vol 9, Iss 1, Pp 1-

    2018  Volume 4

    Abstract: Abstract Prebiotic chemistry, driven by changing environmental parameters provides canonical and a multitude of non-canonical nucleosides. This suggests that Watson-Crick base pairs were selected from a diverse pool of nucleosides in a pre-Darwinian ... ...

    Abstract Abstract Prebiotic chemistry, driven by changing environmental parameters provides canonical and a multitude of non-canonical nucleosides. This suggests that Watson-Crick base pairs were selected from a diverse pool of nucleosides in a pre-Darwinian chemical evolution process.
    Keywords Science ; Q
    Language English
    Publishing date 2018-12-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  8. Article ; Online: Author Correction

    María Arroyo / Florian D. Hastert / Andreas Zhadan / Florian Schelter / Susanne Zimbelmann / Cathia Rausch / Anne K. Ludwig / Thomas Carell / M. Cristina Cardoso

    Nature Communications, Vol 14, Iss 1, Pp 1-

    Isoform-specific and ubiquitination dependent recruitment of Tet1 to replicating heterochromatin modulates methylcytosine oxidation

    2023  Volume 2

    Keywords Science ; Q
    Language English
    Publishing date 2023-01-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  9. Article ; Online: Depletion of pyruvate kinase (PK) activity causes glycolytic intermediate imbalances and reveals a PK-TXNIP regulatory axis

    Anna Nieborak / Saulius Lukauskas / Jordi Capellades / Patricia Heyn / Gabriela Silva Santos / Karsten Motzler / Anja Zeigerer / Romina Bester / Ulrike Protzer / Florian Schelter / Mirko Wagner / Thomas Carell / Alexander Hruscha / Bettina Schmid / Oscar Yanes / Robert Schneider

    Molecular Metabolism, Vol 74, Iss , Pp 101748- (2023)

    2023  

    Abstract: Objective: Cancer cells convert more glucose into lactate than healthy cells, what contributes to their growth advantage. Pyruvate kinase (PK) is a key rate limiting enzyme in this process, what makes it a promising potential therapeutic target. However, ...

    Abstract Objective: Cancer cells convert more glucose into lactate than healthy cells, what contributes to their growth advantage. Pyruvate kinase (PK) is a key rate limiting enzyme in this process, what makes it a promising potential therapeutic target. However, currently it is still unclear what consequences the inhibition of PK has on cellular processes. Here, we systematically investigate the consequences of PK depletion for gene expression, histone modifications and metabolism. Methods: Epigenetic, transcriptional and metabolic targets were analysed in different cellular and animal models with stable knockdown or knockout of PK. Results: Depleting PK activity reduces the glycolytic flux and causes accumulation of glucose-6-phosphate (G6P). Such metabolic perturbation results in stimulation of the activity of a heterodimeric pair of transcription factors MondoA and MLX but not in a major reprogramming of the global H3K9ac and H3K4me3 histone modification landscape. The MondoA:MLX heterodimer upregulates expression of thioredoxin-interacting protein (TXNIP) – a tumour suppressor with multifaceted anticancer activity. This effect of TXNIP upregulation extends beyond immortalised cancer cell lines and is applicable to multiple cellular and animal models. Conclusions: Our work shows that actions of often pro-tumorigenic PK and anti-tumorigenic TXNIP are tightly linked via a glycolytic intermediate. We suggest that PK depletion stimulates the activity of MondoA:MLX transcription factor heterodimers and subsequently, increases cellular TXNIP levels. TXNIP-mediated inhibition of thioredoxin (TXN) can reduce the ability of cells to scavenge reactive oxygen species (ROS) leading to the oxidative damage of cellular structures including DNA. These findings highlight an important regulatory axis affecting tumour suppression mechanisms and provide an attractive opportunity for combination cancer therapies targeting glycolytic activity and ROS-generating pathways.
    Keywords Pyruvate kinase ; Cancer ; ROS ; Glycolysis ; Thioredoxin-interacting protein ; Arrestins ; Internal medicine ; RC31-1245
    Subject code 570
    Language English
    Publishing date 2023-08-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  10. Article ; Online: Isoform-specific and ubiquitination dependent recruitment of Tet1 to replicating heterochromatin modulates methylcytosine oxidation

    María Arroyo / Florian D. Hastert / Andreas Zhadan / Florian Schelter / Susanne Zimbelmann / Cathia Rausch / Anne K. Ludwig / Thomas Carell / M. Cristina Cardoso

    Nature Communications, Vol 13, Iss 1, Pp 1-

    2022  Volume 28

    Abstract: A short isoform of the Tet1 enzyme (Tet1s) that oxidizes the DNA 5-methylcytosine (5mC) mark is overexpressed in tumors. Here the authors show Tet1s, but not full length Tet1, changes localization over the cell cycle upon ubiquitination and Uhrf1 ... ...

    Abstract A short isoform of the Tet1 enzyme (Tet1s) that oxidizes the DNA 5-methylcytosine (5mC) mark is overexpressed in tumors. Here the authors show Tet1s, but not full length Tet1, changes localization over the cell cycle upon ubiquitination and Uhrf1 interaction and is targeted to heterochromatin during S-phase. This leads to 5mC oxidation and loss of DNA methylation in heterochromatin.
    Keywords Science ; Q
    Language English
    Publishing date 2022-09-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

To top