O'connor Michael
School of Biological Sciences, University of Missouri-Kansas City, 5007 Rockhill Rd., Kansas City, MO 64110, USA.
Mol Genet Genomics. 2007 Sep;278(3):307-15. doi: 10.1007/s00438-007-0252-y. Epub 2007 Jun 13.
A1916 in 23S rRNA is located in one of the major intersubunit bridges of the 70S ribosome. Deletion of A1916 disrupts the intersubunit bridge B2a, promotes misreading of the genetic code and is lethal. In a genetic selection for suppressor mutations, two base substitutions in 16S rRNA were recovered that restored viability and also allowed expression of DeltaA1916-associated capreomycin resistance. These mutations were G1048A in helix 34 and U1471C in helix 44. Restoration of function is incomplete, however, and the double mutants are slow-growing, defective in subunit association and support high levels of translational errors. In contrast, none of these parameters is affected by the single 16S suppressor mutations. U1471C likely affects another intersubunit contact, bridge B6, suggesting that interactions between different bridges and cross-talk between subunits contributes to ribosomal function.
23S rRNA中的A1916位于70S核糖体主要亚基间桥之一。A1916的缺失会破坏亚基间桥B2a,导致遗传密码错读,且具有致死性。在对抑制子突变的遗传筛选中,在16S rRNA中发现了两个碱基替换,它们恢复了细胞活力,并且还使与ΔA1916相关的卷曲霉素抗性得以表达。这些突变分别是位于螺旋34的G1048A和位于螺旋44的U1471C。然而,功能恢复并不完全,双突变体生长缓慢,亚基结合存在缺陷,并且支持高水平的翻译错误。相比之下,这些参数均不受单个16S抑制子突变的影响。U1471C可能影响另一个亚基间接触,即桥B6,这表明不同桥之间的相互作用以及亚基之间的相互影响有助于核糖体功能。