NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE140051 Query DataSets for GSE140051
Status Public on Jan 07, 2022
Title Non-canonical base modifications of bacterial origin in a eukaryotic genome [RNA-seq]
Organism Adineta vaga
Experiment type Expression profiling by high throughput sequencing
Summary Methylation of cytosines at the 5th carbon position of the aromatic ring has long been regarded as the predominant type of DNA base modification in eukaryotes. Often called “the fifth base”, C5-methylcytosine (5mC) plays an important role in genome defense against mobile genetic elements, and is mostly associated with transcriptional silencing, establishment of the closed chromatin configuration, and repressive histone modifications. Recently, another type of DNA modification, N6-methyladenine (6mA), has been added to the repertoire of modified bases in eukaryotic DNA, and was mostly linked to elevated transcription levels. In prokaryotes, 5mC and 6mA typically constitute components of restriction-modification (R-M) systems, along with N4-methylcytosine (4mC), which so far has been confined to bacteria. Here we report the first case of 4mC occurrence in eukaryotic DNA. We find that bdelloid rotifers, small freshwater invertebrates known for their ability to reproduce clonally and to acquire genes from non-metazoan sources, lack the canonical eukaryotic C5-methyltransferases but instead encode an amino-methyltransferase of bacterial origin, N4CMT, which is present in all bdelloid families separated by tens of millions of years of evolution. The recombinant N4CMT introduces 4mC into genomic DNA in vivo and in vitro. Using SMRT-seq (PRJNA558051), MeDIP-seq, ChIP-seq, and RNA-seq, we examined genome-wide distribution of non-canonical base modifications over annotated genomic features and observed an excess of 4mC in silenced transposable elements and certain tandem repeats, while 6mA tends to associate with transcribed genes and active chromatin. The presence of the chromodomain in N4CMT explains its affinity for repressive histone marks, H3K9me3 and especially H3K27me3. Our results expand the known repertoire of eukaryotic base modifications, shed light on the process of recruitment of methyl groups as epigenetic marks in DNA, and highlight the role of horizontal gene transfer as an important driver of evolutionary innovation in eukaryotes.
 
Overall design Examination of 4mC and 6mA DNA methylation with MeDIP-seq, ChIP-seq, and RNA-seq in two Adineta vaga strains (reference and L1).
 
Contributor(s) Rodriguez F, Yushenova IA, DiCorpo D, Arkhipova IR
Citation(s) 35228526
NIH grant(s)
Grant ID Grant title Affiliation Name
R01 GM111917 Horizontal gene transfer as a source of evolutionary innovation in metazoans MARINE BIOLOGICAL LABORATORY Irina Arkhipova
Submission date Nov 06, 2019
Last update date Mar 30, 2022
Contact name Irina Arkhipova
E-mail(s) iarkhipova@mbl.edu
Organization name Marine Biological Laboratory
Department Josephine Bay Paul Center
Lab Arkhipova Lab
Street address 7 MBL St
City Woods Hole
State/province MA
ZIP/Postal code 02543
Country USA
 
Platforms (2)
GPL27727 Illumina NextSeq 500 (Adineta vaga)
GPL27729 Illumina NovaSeq 6000 (Adineta vaga)
Samples (5)
GSM4152122 AvL1-RNA-Rep1
GSM4152123 AvL1-RNA-Rep2
GSM4152124 Av-RNA-Rep1
This SubSeries is part of SuperSeries:
GSE140052 Non-canonical base modifications of bacterial origin in a eukaryotic genome
Relations
BioProject PRJNA588092
SRA SRP228822

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE140051_Av-RNA-Rep_GeneID_count.txt.gz 315.6 Kb (ftp)(http) TXT
GSE140051_AvL1-RNA-Rep_GeneID_count.txt.gz 368.1 Kb (ftp)(http) TXT
GSE140051_AvL1_GeneID_hints-braker.cds.fasta.gz 26.9 Mb (ftp)(http) FASTA
GSE140051_AvL1_GeneID_hints-braker.gff3.gz 11.4 Mb (ftp)(http) GFF3
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap