Tarn W Y, Lee K R, Cheng S C
Institute of Molecular Biology, Academia Sinica, Nankang, Taiwan, Republic of China.
Proc Natl Acad Sci U S A. 1993 Nov 15;90(22):10821-5. doi: 10.1073/pnas.90.22.10821.
During assembly of the spliceosome, the U4 small nuclear RNA (snRNA) interacts with the spliceosome as a preformed U4/U6-U5 triple small nuclear ribonucleoprotein (snRNP) complex. Subsequently, U4 becomes loosely associated with the spliceosome, whereas U5 and U6 remain tightly associated, suggesting unwinding of the U4/U6 duplex. We show that this step of the assembly process can be blocked by limiting the ATP concentration in the splicing reaction. We also show that the yeast precursor mRNA processing protein PRP19 becomes associated with the spliceosome during this transition. Thus, PRP19 may function in this step of spliceosome assembly.
在剪接体组装过程中,U4小核RNA(snRNA)作为预先形成的U4/U6-U5三聚体小核糖核蛋白(snRNP)复合体与剪接体相互作用。随后,U4与剪接体松散结合,而U5和U6仍紧密结合,这表明U4/U6双链体发生了解旋。我们发现,通过限制剪接反应中的ATP浓度,可以阻断组装过程的这一步骤。我们还发现,酵母前体mRNA加工蛋白PRP19在这一转变过程中与剪接体结合。因此,PRP19可能在剪接体组装的这一步骤中发挥作用。