Biochemical Characterization of the DASH‐Type Cryptochrome CryD From Fusarium fujikuroi. (11th September 2015)
- Record Type:
- Journal Article
- Title:
- Biochemical Characterization of the DASH‐Type Cryptochrome CryD From Fusarium fujikuroi. (11th September 2015)
- Main Title:
- Biochemical Characterization of the DASH‐Type Cryptochrome CryD From Fusarium fujikuroi
- Authors:
- Castrillo, Marta
Bernhardt, Adrian
Ávalos, Javier
Batschauer, Alfred
Pokorny, Richard - Abstract:
- Abstract: Proteins from the cryptochrome/photolyase family utilize UV‐A, blue or even red light to achieve such diverse functions as repair of DNA lesions by photolyases and signaling by cryptochromes. DASH‐type cryptochromes retained the ability to repair cyclobutane pyrimidine dimers (CPDs) in single‐stranded DNA regions in vitro . However, most organisms possess conventional CPD photolyases responsible for repair of these lesions in vivo . Recent work showed that the DASH‐type cryptochrome CryD plays a regulatory role in diverse light‐dependent processes in Fusarium fujikuroi . Here, we report our in vitro studies on heterologously expressed Ff CryD. The purified protein contains N 5, N 10 ‐methenyltetrahydrofolate and flavin adenine dinucleotide as cofactors. Photoreduction and DNA photorepair experiments confirmed that Ff CryD is active in light‐driven electron transfer processes. However, the protein showed comparable affinities for CPD‐comprising and undamaged DNA probes. Surprisingly, after purification, full‐length Ff CryD as well as a truncated version containing only the PHR domain bound RNA which influenced their behavior in vitro . Moreover, binding of Ff CryD to RNA indicates a putative role in RNA metabolism or in posttranscriptional control of gene expression. Abstract : The study biochemically characterizes the heterologously expressed and purified DASH‐type cryptochrome CryD that plays regulatory roles in Fusarium fujikuroi . As an example, CryD inhibitsAbstract: Proteins from the cryptochrome/photolyase family utilize UV‐A, blue or even red light to achieve such diverse functions as repair of DNA lesions by photolyases and signaling by cryptochromes. DASH‐type cryptochromes retained the ability to repair cyclobutane pyrimidine dimers (CPDs) in single‐stranded DNA regions in vitro . However, most organisms possess conventional CPD photolyases responsible for repair of these lesions in vivo . Recent work showed that the DASH‐type cryptochrome CryD plays a regulatory role in diverse light‐dependent processes in Fusarium fujikuroi . Here, we report our in vitro studies on heterologously expressed Ff CryD. The purified protein contains N 5, N 10 ‐methenyltetrahydrofolate and flavin adenine dinucleotide as cofactors. Photoreduction and DNA photorepair experiments confirmed that Ff CryD is active in light‐driven electron transfer processes. However, the protein showed comparable affinities for CPD‐comprising and undamaged DNA probes. Surprisingly, after purification, full‐length Ff CryD as well as a truncated version containing only the PHR domain bound RNA which influenced their behavior in vitro . Moreover, binding of Ff CryD to RNA indicates a putative role in RNA metabolism or in posttranscriptional control of gene expression. Abstract : The study biochemically characterizes the heterologously expressed and purified DASH‐type cryptochrome CryD that plays regulatory roles in Fusarium fujikuroi . As an example, CryD inhibits the light‐induced accumulation of a red polyketide pigment bikaverin in F. fujikuroi mycelia. Colonies of F. fujikuroi wild‐type strain (Wild type) and of a representative CryD null‐mutant strain (Δ cryD ) grown for 7 days at 30°C on a minimal medium with low nitrogen content in white light (Light) are colored differently whereas colonies of the two strains grown in darkness (Dark) show the same color. … (more)
- Is Part Of:
- Photochemistry and photobiology. Volume 91:Number 6(2015:Nov./Dec.)
- Journal:
- Photochemistry and photobiology
- Issue:
- Volume 91:Number 6(2015:Nov./Dec.)
- Issue Display:
- Volume 91, Issue 6 (2015)
- Year:
- 2015
- Volume:
- 91
- Issue:
- 6
- Issue Sort Value:
- 2015-0091-0006-0000
- Page Start:
- 1356
- Page End:
- 1367
- Publication Date:
- 2015-09-11
- Subjects:
- Photochemistry -- Periodicals
Light -- Physiological effect -- Periodicals
541.35 - Journal URLs:
- http://www.blackwellpublishing.com/journal.asp?ref=0031-8655&site=1 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/php.12501 ↗
- Languages:
- English
- ISSNs:
- 0031-8655
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6465.985000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 9879.xml