DNA-Binding Properties of a Novel Crenarchaeal Chromatin-Organizing Protein in Sulfolobus acidocaldarius

被引:4
作者
Lemmens, Liesbeth [1 ]
Wang, Kun [2 ]
Ruykens, Ebert [1 ]
Van Tinh Nguyen [1 ,4 ]
Lindas, Ann-Christin [2 ]
Willaert, Ronnie [3 ]
Couturier, Mohea [1 ]
Peeters, Eveline [1 ]
机构
[1] Vrije Univ Brussel, Dept Bioengn Sci, Res Grp Microbiol, B-1050 Brussels, Belgium
[2] Stockholm Univ, Wenner Gren Inst, Dept Mol Biosci, S-11597 Stockholm, Sweden
[3] Vrije Univ Brussel, Dept Bioengn Sci, Int Joint Res Grp VUB EFPL NanoBiotechnol & NanoM, Alliance Res Grp VUB UGent NanoMicrobiol,Res Grp, B-1050 Brussels, Belgium
[4] Katholieke Univ Leuven, Div Soil & Water Management, B-3001 Leuven, Belgium
关键词
archaea; Sulfolobus; nucleoid-associated protein; DNA binding; atomic force microscopy; chromatin structure; NUCLEOID-ASSOCIATED PROTEINS; CRYSTAL-STRUCTURE; ARCHAEAL; REGULATOR; TRANSCRIPTION; ORGANIZATION; COMPACTION; GENOME; CREN7;
D O I
10.3390/biom12040524
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In archaeal microorganisms, the compaction and organization of the chromosome into a dynamic but condensed structure is mediated by diverse chromatin-organizing proteins in a lineage-specific manner. While many archaea employ eukaryotic-type histones for nucleoid organization, this is not the case for the crenarchaeal model species Sulfolobus acidocaldarius and related species in Sulfolobales, in which the organization appears to be mostly reliant on the action of small basic DNA-binding proteins. There is still a lack of a full understanding of the involved proteins and their functioning. Here, a combination of in vitro and in vivo methodologies is used to study the DNA-binding properties of Sul12a, an uncharacterized small basic protein conserved in several Sulfolobales species displaying a winged helix-turn-helix structural motif and annotated as a transcription factor. Genome-wide chromatin immunoprecipitation and target-specific electrophoretic mobility shift assays demonstrate that Sul12a of S. acidocaldarius interacts with DNA in a non-sequence specific manner, while atomic force microscopy imaging of Sul12a-DNA complexes indicate that the protein induces structural effects on the DNA template. Based on these results, and a contrario to its initial annotation, it can be concluded that Sul12a is a novel chromatin-organizing protein.
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页数:15
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