TY - JOUR
T1 - Attention-based multi-label neural networks for integrated prediction and interpretation of twelve widely occurring RNA modifications
AU - Song, Zitao
AU - Huang, Daiyun
AU - Song, Bowen
AU - Chen, Kunqi
AU - Song, Yiyou
AU - Liu, Gang
AU - Su, Jionglong
AU - Magalhães, João Pedro de
AU - Rigden, Daniel J.
AU - Meng, Jia
N1 - Funding Information:
The authors would like to thank Prof. Alex Freitas from the University of Kent at Canterbury for his insightful suggestions and comments. This work has been supported by the National Natural Science Foundation of China [31671373]; XJTLU Key Program Special Fund [KSF-T-01]. This work is partially supported by the AI University Research Center through XJTLU Key Program Special Fund (KSF-P-02).
Publisher Copyright:
© 2021, The Author(s).
PY - 2021/12/1
Y1 - 2021/12/1
N2 - Recent studies suggest that epi-transcriptome regulation via post-transcriptional RNA modifications is vital for all RNA types. Precise identification of RNA modification sites is essential for understanding the functions and regulatory mechanisms of RNAs. Here, we present MultiRM, a method for the integrated prediction and interpretation of post-transcriptional RNA modifications from RNA sequences. Built upon an attention-based multi-label deep learning framework, MultiRM not only simultaneously predicts the putative sites of twelve widely occurring transcriptome modifications (m6A, m1A, m5C, m5U, m6Am, m7G, Ψ, I, Am, Cm, Gm, and Um), but also returns the key sequence contents that contribute most to the positive predictions. Importantly, our model revealed a strong association among different types of RNA modifications from the perspective of their associated sequence contexts. Our work provides a solution for detecting multiple RNA modifications, enabling an integrated analysis of these RNA modifications, and gaining a better understanding of sequence-based RNA modification mechanisms.
AB - Recent studies suggest that epi-transcriptome regulation via post-transcriptional RNA modifications is vital for all RNA types. Precise identification of RNA modification sites is essential for understanding the functions and regulatory mechanisms of RNAs. Here, we present MultiRM, a method for the integrated prediction and interpretation of post-transcriptional RNA modifications from RNA sequences. Built upon an attention-based multi-label deep learning framework, MultiRM not only simultaneously predicts the putative sites of twelve widely occurring transcriptome modifications (m6A, m1A, m5C, m5U, m6Am, m7G, Ψ, I, Am, Cm, Gm, and Um), but also returns the key sequence contents that contribute most to the positive predictions. Importantly, our model revealed a strong association among different types of RNA modifications from the perspective of their associated sequence contexts. Our work provides a solution for detecting multiple RNA modifications, enabling an integrated analysis of these RNA modifications, and gaining a better understanding of sequence-based RNA modification mechanisms.
UR - http://www.scopus.com/inward/record.url?scp=85109007105&partnerID=8YFLogxK
U2 - 10.1038/s41467-021-24313-3
DO - 10.1038/s41467-021-24313-3
M3 - Article
C2 - 34188054
AN - SCOPUS:85109007105
SN - 2041-1723
VL - 12
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 4011
ER -