2022
DOI: 10.1016/j.molcel.2021.11.003
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Transcription-wide mapping of dihydrouridine reveals that mRNA dihydrouridylation is required for meiotic chromosome segregation

Abstract: Highlights d Rho-seq detects a range of RNA modifications through differential rhodamine labeling d The dihydrouridine tRNA modification is also present on fission yeast mRNAs d Dihydrouridine on the tubulin mRNA is required for meiotic chromosome segregation d Tubulin mRNA dihydrouridylation is evolutionarily conserved from yeast to human

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Cited by 48 publications
(78 citation statements)
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“…Until recently, the dihydrouridine (D) RNA modification was exclusively studied within the context of tRNA and rRNA biology. However, preliminary data from our lab and elsewhere led us to consider the possibility that other RNA species could also be dihydrouridilated ( Dudin et al., 2017 ; Fauquenoy et al., 2018 ; Finet et al., 2022 ). To assess whether D extends beyond tRNA is particularly challenging given the close resemblance of D to the canonical nucleotide U.…”
Section: Before You Beginmentioning
confidence: 99%
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“…Until recently, the dihydrouridine (D) RNA modification was exclusively studied within the context of tRNA and rRNA biology. However, preliminary data from our lab and elsewhere led us to consider the possibility that other RNA species could also be dihydrouridilated ( Dudin et al., 2017 ; Fauquenoy et al., 2018 ; Finet et al., 2022 ). To assess whether D extends beyond tRNA is particularly challenging given the close resemblance of D to the canonical nucleotide U.…”
Section: Before You Beginmentioning
confidence: 99%
“…We reasoned that regardless of the fluorescent properties of rhodamine, its incorporation should interfere with reverse transcription (RT), leaving a footprint that can be exploited to indirectly observe the presence D. In earlier epitranscriptomic studies, the concept of RT stop footprint was successfully applied to the detection of pseudouridine ( Schwartz et al., 2014 ), inosine ( Suzuki et al., 2015 ) and m 1 A ( Li et al., 2017 ; Safra et al., 2017 ). Similarly, by combining rhodamine labeling of the D modification with high-throughput sequencing, we developed Rho-seq, a method to assess the presence of D at the transcriptome-wide scale ( Finet et al., 2022 ).…”
Section: Before You Beginmentioning
confidence: 99%
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