A primer for junior trainees: Recognition of RNA modifications by RNA-binding proteins

被引:0
作者
Angelo, Murphy [1 ]
Bhargava, Yash [1 ]
Aoki, Scott Takeo [1 ]
机构
[1] Indiana Univ Purdue Univ Indianapolis, Sch Med, Dept Biochem & Mol Biol, Indianapolis, IN 46202 USA
关键词
review; RNA; RNA modifications; RNA-binding proteins; RNA-protein interactions; MESSENGER-RNA; CRYSTAL-STRUCTURE; WIDE IDENTIFICATION; STRUCTURAL BASIS; DOMAIN; M(6)A; PUMILIO; SPECIFICITY; METHYLTRANSFERASE; MECHANISM;
D O I
10.1002/bmb.21854
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
The complexity of RNA cannot be fully expressed with the canonical A, C, G, and U alphabet. To date, over 170 distinct chemical modifications to RNA have been discovered in living systems. RNA modifications can profoundly impact the cellular outcomes of messenger RNAs (mRNAs), transfer and ribosomal RNAs, and noncoding RNAs. Additionally, aberrant RNA modifications are associated with human disease. RNA modifications are a rising topic within the fields of biochemistry and molecular biology. The role of RNA modifications in gene regulation, disease pathogenesis, and therapeutic applications increasingly captures the attention of the scientific community. This review aims to provide undergraduates, junior trainees, and educators with an appreciation for the significance of RNA modifications in eukaryotic organisms, alongside the skills required to identify and analyze fundamental RNA-protein interactions. The pumilio RNA-binding protein and YT521-B homology (YTH) family of modified RNA-binding proteins serve as examples to highlight the fundamental biochemical interactions that underlie the specific recognition of both unmodified and modified ribonucleotides, respectively. By instilling these foundational, textbook concepts through practical examples, this review contributes an analytical toolkit that facilitates engagement with RNA modifications research at large.
引用
收藏
页码:701 / 710
页数:10
相关论文
共 82 条
  • [1] Concepts and methods for transcriptome-wide prediction of chemical messenger RNA modifications with machine learning
    Acera Mateos, Pablo
    Zhou, You
    Zarnack, Kathi
    Eyras, Eduardo
    [J]. BRIEFINGS IN BIOINFORMATICS, 2023, 24 (03)
  • [2] Structural basis of the RNA-binding specificity of human U1A protein
    Allain, FHT
    Howe, PWA
    Neuhaus, D
    Varani, G
    [J]. EMBO JOURNAL, 1997, 16 (18) : 5764 - 5774
  • [3] Structure-based analysis of Protein-RNA interactions using the program ENTANGLE
    Allers, J
    Shamoo, Y
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2001, 311 (01) : 75 - 86
  • [4] Inosine in DNA and RNA
    Alseth, Ingrun
    Dalhus, Bjorn
    Bjoras, Magnar
    [J]. CURRENT OPINION IN GENETICS & DEVELOPMENT, 2014, 26 : 116 - 123
  • [5] Anderson JT, 2005, TOP CURR GENET, V12, P121, DOI 10.1007/b106364
  • [6] C. elegans germ granules require both assembly and localized regulators for mRNA repression
    Aoki, Scott Takeo
    Lynch, Tina R.
    Crittenden, Sarah L.
    Bingman, Craig A.
    Wickens, Marvin
    Kimble, Judith
    [J]. NATURE COMMUNICATIONS, 2021, 12 (01)
  • [7] RNA-protein interactions: disorder, moonlighting and junk contribute to eukaryotic complexity
    Balcerak, Anna
    Trebinska-Stryjewska, Alicja
    Konopinski, Ryszard
    Wakula, Maciej
    Grzybowska, Ewa Anna
    [J]. OPEN BIOLOGY, 2019, 9 (06)
  • [8] MODOMICS: a database of RNA modification pathways. 2021 update
    Boccaletto, Pietro
    Stefaniak, Filip
    Ray, Angana
    Cappannini, Andrea
    Mukherjee, Sunandan
    Purta, Elzbieta
    Kurkowska, Malgorzata
    Shirvanizadeh, Niloofar
    Destefanis, Eliana
    Groza, Paula
    Avsar, Gulben
    Romitelli, Antonia
    Pir, Pinar
    Dassi, Erik
    Conticello, Silvestro G.
    Aguilo, Francesca
    Bujnicki, Janusz M.
    [J]. NUCLEIC ACIDS RESEARCH, 2022, 50 (D1) : D231 - D235
  • [9] BOKAR JA, 1994, J BIOL CHEM, V269, P17697
  • [10] A protein-RNA specificity code enables targeted activation of an endogenous human transcript
    Campbell, Zachary T.
    Valley, Cary T.
    Wickens, Marvin
    [J]. NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2014, 21 (08) : 732 - 738