2026-01-13 東京大学
TUT4・Lin28・前駆体let-7 RNAからなる三者複合体構造
<関連情報>
- https://www.k.u-tokyo.ac.jp/information/category/press/0028954.html
- https://www.k.u-tokyo.ac.jp/assets/files/がん抑制マイクロRNA生合成を制御する分子機構を解明_WEB.pdf
- https://academic.oup.com/nar/article/54/1/gkaf1421/8417339
TUT4によるpre-let-7のLin28依存性オリゴウリジル化の機構的洞察 Mechanistic insights into Lin28-dependent oligo-uridylylation of pre-let-7 by TUT4
Xiaojie Han ,Seisuke Yamashita ,Kozo Tomita
Nucleic Acids Research Published:12 January 2026
DOI:https://doi.org/10.1093/nar/gkaf1421
Abstract
Lin28-dependent oligo-uridylylation of precursor let-7 (pre-let-7) by terminal uridylyltransferases 4 and 7 (TUT4/7) represses let-7 expression by blocking Dicer processing, thereby regulating cell differentiation and proliferation. The interaction between the Lin28:pre-let-7 complex and the N-terminal Lin28-interacting module (LIM) of TUT4/7 is required for pre-let-7 oligo-uridylylation by the C-terminal catalytic module (CM). Here, we report the cryogenic electron microscopy structure of human TUT4 complexed with Lin28A and oligo-uridylated pre-let-7, representing the elongation stage of oligo-uridylylation. Structural and biochemical analyses suggest that, after recruitment of pre-let-7 to the LIM through interactions between its terminal stem-loop and Lin28A, the CM associates with the LIM through protein–protein interactions. The double-stranded stem region of pre-let-7 is surrounded by the CM and LIM, the upper portion of the duplex unwinds, and the 3′ end of pre-let-7 is positioned in the CM catalytic site for the initiation of oligo-uridylylation. At the oligo-uridylylation stage, the CM finger domain clamps the double-stranded region of pre-let-7, thereby further stabilizing the pre-let-7:TUT4 complex, enabling processive elongation of the uridine tail by the CM. Thus, the LIM functions as a stable anchor, working together with Lin28A to ensure efficient and processive oligo-uridylylation of pre-let-7.
