57 research outputs found
Auf abgrĂŒndigen Pfaden in die Sozialwissenschaft?
In der Lehre zur EinfĂŒhrung in qualitative Forschungsmethoden, meist zu Beginn eines wissenschaftlichen Studiums, sehen sich Dozierende zuweilen mit einer studentischen Skepsis gegenĂŒber den pluralistischen WahrheitsansprĂŒchen sozialer Wirklichkeiten und ebenso gegenĂŒber abstrahierten Analyseergebnissen einer qualitativ forschenden Sozialwissenschaft konfrontiert. Anhand einer ausfĂŒhrlichen Reflexion ĂŒber GĂŒltigkeit und Legitimation von WahrheitsansprĂŒchen sozialwissenschaftlicher Methoden versucht dieser Beitrag, derlei artikulierte Vorbehalte systematisch zu fassen und auf der Grundlage eigener Lehrerfahrungen didaktische Erwiderungsmöglichkeiten vorzustellen, um Studierenden eine konstruktivistisch-sozialwissenschaftliche Haltung nahezubringen.Lecturers frequently have to deal with skepticism from undergraduates whilst teaching qualitative research methods. This skepticism either refers to the pluralistic claims of truth within the variety of social realities or to the analytic results of qualitative inquiries. Based on personal teaching experiences, this article tries to systematically summarize reservations that have been articulated by students and wants to further present didactic possibilities of rejoinders. The basis of these thoughts is an extensive reflection of the foundational principles of social sciences
Untersuchungen zum Einfluss von Sulforaphan auf die DNA-Einzelstrangbruch- und Nukleotidexzisionsreparatur
Eine Risikobewertung von Broccoli-basierten NahrungsergÀnzungsmitteln fehlt bis dato. Die vorliegende Arbeit leistet in diesem Kontext nun erstmals einen kritischen Beitrag zur Auswirkung der bioaktiven Substanz Sulforaphan (SFN) auf essentielle DNA-Reparaturprozesse, die anhand der Prozessierung und Reparatur zweier ModelllÀsionen in Zellkulturen beurteilt wurden. Es zeigte sich, dass SFN beide Reparaturwege inhibiert und Zink-bindende Strukturen dabei potentielle Angriffspunkte darstellen
BET inhibition induces HEXIM1- and RAD51-dependent conflicts between transcription and replication
Summary: BET bromodomain proteins are required for oncogenic transcription activities, and BET inhibitors have been rapidly advanced into clinical trials. Understanding the effects of BET inhibition on processes such as DNA replication will be important for future clinical applications. Here, we show that BET inhibition, and specifically inhibition of BRD4, causes replication stress through a rapid overall increase in RNA synthesis. We provide evidence that BET inhibition acts by releasing P-TEFb from its inhibitor HEXIM1, promoting interference between transcription and replication. Unusually, these transcription-replication conflicts do not activate the ATM/ATR-dependent DNA damage response but recruit the homologous recombination factor RAD51. Both HEXIM1 and RAD51 promote BET inhibitor-induced fork slowing but also prevent a DNA damage response. Our data suggest that BET inhibitors slow replication through concerted action of transcription and recombination machineries and shed light on the importance of replication stress in the action of this class of experimental cancer drugs. : Bowry et al. show that BET inhibitors, emerging cancer therapeutics that target transcription programs, cause conflicts between transcription and replication by deregulating P-TEFb. These conflicts recruit the homologous recombination factor RAD51, which slows down replication and suppresses DNA damage. This highlights the importance of replication stress for BET inhibitor treatment. Keywords: JQ1, I-BET151, BRD4, P-TEFb, homologous recombination, replication fork, replication stress, DNA damage, cance
BPDE-induced genotoxicity: relationship between DNA adducts, mutagenicity in the in vitro PIG-A assay, and the transcriptional response to DNA damage in TK6 cells
Adenovirus E1B 55-kilodalton protein targets SMARCAL1 for degradation during infection and modulates cellular DNA replication
PARP1 and PARP2 stabilise replication forks at base excision repair intermediates through Fbh1-dependent Rad51 regulation
PARP1 regulates the repair of DNA single strand breaks (SSBs) generated directly,
or during base excision repair (BER). However, the role of PARP2 in these and other
repair mechanisms is unknown. Here, we report a requirement for PARP2 in
stabilising replication forks that encounter BER intermediates through Fbh1-
dependent regulation of Rad51. Whilst PARP2 is dispensable for tolerance of cells to
SSBs or homologous recombination dysfunction, it is redundant with PARP1 in BER.
Therefore, combined disruption of PARP1 and PARP2 leads to defective BER,
resulting in elevated levels of replication associated DNA damage due to an inability
to stabilise Rad51 at damaged replication forks and prevent uncontrolled DNA
resection. Together, our results demonstrate how PARP1 and PARP2 regulate two
independent, but intrinsically linked aspects of DNA base damage tolerance by
promoting BER directly, and through stabilising replication forks that encounter BER
intermediates
PrimPol-dependent single-stranded gap formation mediates homologous recombination at bulky DNA adducts
Stalled replication forks can be restarted and repaired by RAD51-mediated homologous recombination (HR), but HR can also perform post-replicative repair after bypass of the obstacle. Bulky DNA adducts are important replication-blocking lesions, but it is unknown whether they activate HR at stalled forks or behind ongoing forks. Using mainly BPDE-DNA adducts as model lesions, we show that HR induced by bulky adducts in mammalian cells predominantly occurs at post-replicative gaps formed by the DNA/RNA primase PrimPol. RAD51 recruitment under these conditions does not result from fork stalling, but rather occurs at gaps formed by PrimPol re-priming and resection by MRE11 and EXO1. In contrast, RAD51 loading at double-strand breaks does not require PrimPol. At bulky adducts, PrimPol promotes sister chromatid exchange and genetic recombination. Our data support that HR at bulky adducts in mammalian cells involves post-replicative gap repair and define a role for PrimPol in HR-mediated DNA damage tolerance
The genetic interaction network of CCW12, a Saccharomyces cerevisiae gene required for cell wall integrity during budding and formation of mating projections
<p>Abstract</p> <p>Background</p> <p>Mannoproteins construct the outer cover of the fungal cell wall. The covalently linked cell wall protein Ccw12p is an abundant mannoprotein. It is considered as crucial structural cell wall component since in baker's yeast the lack of <it>CCW12 </it>results in severe cell wall damage and reduced mating efficiency.</p> <p>Results</p> <p>In order to explore the function of <it>CCW12</it>, we performed a Synthetic Genetic Analysis (SGA) and identified genes that are essential in the absence of <it>CCW12</it>. The resulting interaction network identified 21 genes involved in cell wall integrity, chitin synthesis, cell polarity, vesicular transport and endocytosis. Among those are <it>PFD1</it>, <it>WHI3</it>, <it>SRN2</it>, <it>PAC10</it>, <it>FEN1 </it>and <it>YDR417C</it>, which have not been related to cell wall integrity before. We correlated our results with genetic interaction networks of genes involved in glucan and chitin synthesis. A core of genes essential to maintain cell integrity in response to cell wall stress was identified. In addition, we performed a large-scale transcriptional analysis and compared the transcriptional changes observed in mutant <it>ccw12</it>Î with transcriptomes from studies investigating responses to constitutive or acute cell wall damage. We identified a set of genes that are highly induced in the majority of the mutants/conditions and are directly related to the cell wall integrity pathway and cell wall compensatory responses. Among those are <it>BCK1</it>, <it>CHS3</it>, <it>EDE1</it>, <it>PFD1</it>, <it>SLT2 </it>and <it>SLA1 </it>that were also identified in the SGA. In contrast, a specific feature of mutant <it>ccw12</it>Î is the transcriptional repression of genes involved in mating. Physiological experiments substantiate this finding. Further, we demonstrate that Ccw12p is present at the cell periphery and highly concentrated at the presumptive budding site, around the bud, at the septum and at the tip of the mating projection.</p> <p>Conclusions</p> <p>The combination of high throughput screenings, phenotypic analyses and localization studies provides new insight into the function of Ccw12p. A compensatory response, culminating in cell wall remodelling and transport/recycling pathways is required to buffer the loss of <it>CCW12</it>. Moreover, the enrichment of Ccw12p in bud, septum and mating projection is consistent with a role of Ccw12p in preserving cell wall integrity at sites of active growth.</p> <p>The microarray data produced in this analysis have been submitted to NCBI GEO database and GSE22649 record was assigned.</p
The selective cytotoxicity of the alkenyl glucosinolate hydrolysis products and their presence in Brassica vegetables.
Repriming DNA synthesis: an intrinsic restart pathway that maintains efficient genome replication
To bypass a diverse range of fork stalling impediments encountered during genome replication, cells possess a variety of DNA damage tolerance (DDT) mechanisms including translesion synthesis, template switching, and fork reversal. These pathways function to bypass obstacles and allow efficient DNA synthesis to be maintained. In addition, lagging strand obstacles can also be circumvented by downstream priming during Okazaki fragment generation, leaving gaps to be filled post-replication. Whether repriming occurs on the leading strand has been intensely debated over the past half-century. Early studies indicated that both DNA strands were synthesised discontinuously. Although later studies suggested that leading strand synthesis was continuous, leading to the preferred semi-discontinuous replication model. However, more recently it has been established that replicative primases can perform leading strand repriming in prokaryotes. An analogous fork restart mechanism has also been identified in most eukaryotes, which possess a specialist primase called PrimPol that conducts repriming downstream of stalling lesions and structures. PrimPol also plays a more general role in maintaining efficient fork progression. Here, we review and discuss the historical evidence and recent discoveries that substantiate repriming as an intrinsic replication restart pathway for maintaining efficient genome duplication across all domains of life
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