TY - JOUR
T1 - The Intersubunit Bridge B1b of the Bacterial Ribosome Facilitates Initiation of Protein Synthesis and Maintenance of Translational Fidelity
AU - Lilleorg, Silva
AU - Reier, Kaspar
AU - Remme, Jaanus
AU - Liiv, Aivar
N1 - Publisher Copyright:
© 2017 Elsevier Ltd
PY - 2017/4/7
Y1 - 2017/4/7
N2 - In bacteria, ribosomal subunits are connected via 12 intersubunit bridges involving RNA–RNA, RNA–protein, and protein–protein interactions. The only protein–protein bridge in the ribosome is ribosomal intersubunit bridge 1b (B1b), which is mainly formed by the bacterial protein L31 (bL31) and connects the head domain of 30S subunit and the central protuberance of the 50S subunit. It is known to be the most dynamic intersubunit bridge. Here, we have evaluated the role of bL31 and thereby the bridge B1b in the working cycle of the ribosome. First, bL31-deficient ribosomes are severely compromised in their ability to ensure translational fidelity particularly in reading frame maintenance in vivo. Second, in the absence of bL31, the rate of initiation is significantly reduced both in vivo and in vitro. Third, polysome profile and subunit reassociation assays demonstrate that bL31 is important for stabilizing subunit joining in vivo and in vitro. Together, our results demonstrate that bL31 is important for determining translational fidelity and stabilizing subunit association. We conclude that the only protein–protein intersubunit bridge of the bacterial ribosome facilitates translation initiation and is essential for maintaining the reading frame of mRNA translation.
AB - In bacteria, ribosomal subunits are connected via 12 intersubunit bridges involving RNA–RNA, RNA–protein, and protein–protein interactions. The only protein–protein bridge in the ribosome is ribosomal intersubunit bridge 1b (B1b), which is mainly formed by the bacterial protein L31 (bL31) and connects the head domain of 30S subunit and the central protuberance of the 50S subunit. It is known to be the most dynamic intersubunit bridge. Here, we have evaluated the role of bL31 and thereby the bridge B1b in the working cycle of the ribosome. First, bL31-deficient ribosomes are severely compromised in their ability to ensure translational fidelity particularly in reading frame maintenance in vivo. Second, in the absence of bL31, the rate of initiation is significantly reduced both in vivo and in vitro. Third, polysome profile and subunit reassociation assays demonstrate that bL31 is important for stabilizing subunit joining in vivo and in vitro. Together, our results demonstrate that bL31 is important for determining translational fidelity and stabilizing subunit association. We conclude that the only protein–protein intersubunit bridge of the bacterial ribosome facilitates translation initiation and is essential for maintaining the reading frame of mRNA translation.
KW - bL31
KW - Escherichia coli
KW - ribosomal proteins
KW - ribosome subunit association
KW - translational fidelity
UR - http://www.scopus.com/inward/record.url?scp=85014631324&partnerID=8YFLogxK
U2 - 10.1016/j.jmb.2017.02.015
DO - 10.1016/j.jmb.2017.02.015
M3 - Article
C2 - 28238762
AN - SCOPUS:85014631324
SN - 0022-2836
VL - 429
SP - 1067
EP - 1080
JO - Journal of Molecular Biology
JF - Journal of Molecular Biology
IS - 7
ER -