6M1U

Crystal structure of the vertebrate conserved region (VCR) of human METTL16

6M1U の概要

• エントリーDOI: 10.2210/pdb6m1u/pdb
• 分子名称: RNA N6-adenosine-methyltransferase METTL16,RNA N6-adenosine-methyltransferase METTL16 (1 entity in total)
• 機能のキーワード: methyltransferase, rna binding protein
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 19179.48

構造登録者

Aoyama, T.,Yamashita, S.,Tomita, K. (登録日: 2020-02-26, 公開日: 2020-04-01, 最終更新日: 2024-03-27)

主引用文献

Aoyama, T.,Yamashita, S.,Tomita, K.
Mechanistic insights into m6A modification of U6 snRNA by human METTL16.
Nucleic Acids Res., 48:5157-5168, 2020

PubMed Abstract: The N6-methyladenosine modification at position 43 (m6A43) of U6 snRNA is catalyzed by METTL16, and is important for the 5'-splice site recognition by U6 snRNA during pre-mRNA splicing. Human METTL16 consists of the N-terminal methyltransferase domain (MTD) and the C-terminal vertebrate conserved region (VCR). While the MTD has an intrinsic property to recognize a specific sequence in the distinct structural context of RNA, the VCR functions have remained uncharacterized. Here, we present structural and functional analyses of the human METTL16 VCR. The VCR increases the affinity of METTL16 toward U6 snRNA, and the conserved basic region in VCR is important for the METTL16-U6 snRNA interaction. The VCR structure is topologically homologous to the C-terminal RNA binding domain, KA1, in U6 snRNA-specific terminal uridylyl transferase 1 (TUT1). A chimera of the N-terminal MTD of METTL16 and the C-terminal KA1 of TUT1 methylated U6 snRNA more efficiently than the MTD, indicating the functional conservation of the VCR and KA1 for U6 snRNA biogenesis. The VCR interacts with the internal stem-loop (ISL) within U6 snRNA, and this interaction would induce the conformational rearrangement of the A43-containing region of U6 snRNA, thereby modifying the RNA structure to become suitable for productive catalysis by the MTD. Therefore, the MTD and VCR in METTL16 cooperatively facilitate the m6A43 U6 snRNA modification.

PubMed: 32266935
DOI: 10.1093/nar/gkaa227

実験手法

X-RAY DIFFRACTION (2.791 Å)