6 research outputs found
The Reverse Transcription Signature of N-\u3csub\u3e1\u3c/sub\u3e-Methyladenosine in RNA-Seq is Sequence Dependent
The combination of Reverse Transcription (RT) and high-throughput sequencing has emerged as a powerful combination to detect modified nucleotides in RNA via analysis of either abortive RT-products or of the incorporation of mismatched dNTPs into cDNA. Here we simultaneously analyze both parameters in detail with respect to the occurrence of N-1-methyladenosine (m1A) in the template RNA. This naturally occurring modification is associated with structural effects, but it is also known as a mediator of antibiotic resistance in ribosomal RNA. In structural probing experiments with dimethylsulfate, m1A is routinely detected by RT-arrest. A specifically developed RNA-Seq protocol was tailored to the simultaneous analysis of RT-arrest and misincorporation patterns. By application to a variety of native and synthetic RNA preparations, we found a characteristic signature of m1A, which, in addition to an arrest rate, features misincorporation as a significant component. Detailed analysis suggests that the signature depends on RNA structure and on the nature of the nucleotide 3’ of m1A in the template RNA, meaning it is sequence dependent. The RT-signature ofm1Awas used for inspection and confirmation of suspected modification sites and resulted in the identification of hitherto unknown m1A residues in trypanosomal tRNA
Diastereoselectivity of 5‑Methyluridine Osmylation Is Inverted inside an RNA Chain
In
this study, we investigated the reaction of the osmium tetroxide–bipyridine
complex with pyrimidines in RNA. This reagent, which reacts with the
diastereotopic 5–6 double bond, thus leading to the formation
of two diastereomers, was used in the past to label thymidine and
5-methylcytosine in DNA. In light of the growing interest in post-transcriptional
RNA modifications, we addressed the question of whether this reagent
could be used for labeling of the naturally occurring RNA modifications
5-methylcytosine and 5-methyluridine. On nucleoside level, 5-methylcytosine
and 5-methyluridine revealed a 5- and 12-fold preference, respectively,
over their nonmethylated equivalents. Performing the reaction on an
RNA level, we could show that the steric environment of a pentanucleotide
has a major detrimental impact on the reaction rate of osmylation.
Interestingly, this drop in reactivity was due to a dramatic change
in diastereoselectivity, which in turn resulted from impediment of
the preferred attack via the <i>si</i> side. Thus, while
on the nucleoside level, the absolute configuration of the major product
of osmylation of 5-methyluridine was (5<i>R</i>,6<i>S</i>)-5-methyluridine glycol-dioxoosmium-bipyridine, reaction
with an RNA pentanucleotide afforded the corresponding (5<i>S</i>,6<i>R</i>)-diastereomer as the major product. The change
in diastereoselectivity lead to an almost complete loss of selectivity
toward 5-methylcytosine in a pentanucleotide context, while 5-methyluridine
remained about 8 times more reactive than the canonical pyrimidines.
On the basis of these findings, we evaluate the usefulness of osmium
tetroxide–bipyridine as a potential label for the 5-methyluridine
modification in transcriptome-wide studies