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Sarah Röhrig

Researcher at Karlsruhe Institute of Technology

Publications -  7
Citations -  160

Sarah Röhrig is an academic researcher from Karlsruhe Institute of Technology. The author has contributed to research in topics: DNA repair & Helicase. The author has an hindex of 5, co-authored 6 publications receiving 95 citations.

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ZYP1 is required for obligate cross-over formation and cross-over interference in Arabidopsis.

TL;DR: In this article, a combination of T-DNA insertional mutants and targeted CRISPR/Cas mutagenesis was used to generate null mutants of the duplicated Arabidopsis transverse filament genes zyp1a and zyp 1b.
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The RTR Complex Partner RMI2 and the DNA Helicase RTEL1 Are Both Independently Involved in Preserving the Stability of 45S rDNA Repeats in Arabidopsis thaliana.

TL;DR: It is demonstrated that, in Arabidopsis thaliana, RMI2 is involved in the repair of aberrant replication intermediates in root meristems as well as in intrastrand crosslink repair, and loss of suppression of HR does not only lead to a destabilization of rDNA repeats but might be especially deleterious for tissues undergoing multiple cell divisions such as the male germline.
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An Arabidopsis FANCJ helicase homologue is required for DNA crosslink repair and rDNA repeat stability.

TL;DR: A homolog of the Fe-S cluster helicase FANCJ in the model plant Arabidopsis, AtFANCJB, is characterized and shown that it is involved in interstrand CL repair and involved in safeguarding rDNA stability in plants.
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The RecQ-like helicase HRQ1 is involved in DNA crosslink repair in Arabidopsis in a common pathway with the Fanconi anemia-associated nuclease FAN1 and the postreplicative repair ATPase RAD5A.

TL;DR: It is concluded that, as in fungi, AtHRQ1 has a conserved function in DNA excision repair and not only shares pathways with the Fanconi anemia repair factors, but in contrast to fungi also seems to act in a common pathway with postreplicative DNA repair.
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The topoisomerase 3α zinc-finger domain T1 of Arabidopsis thaliana is required for targeting the enzyme activity to Holliday junction-like DNA repair intermediates.

TL;DR: It is concluded that the ZFD T1 is specifically required for targeting the topoisomerase activity to HJ like recombination intermediates to enable their processing in the case of an inactivated enzyme.