Tran Quincy, Roesser James R
Department of Biochemistry, Virginia Commonwealth University, 1101 East Marshall Street, Richmond, Virginia 23298, USA.
Biochemistry. 2003 Feb 4;42(4):951-7. doi: 10.1021/bi026753a.
Alternative splicing is an important mechanism for the regulation of gene expression. The mammalian calcitonin/calcitonin gene-related peptide (CGRP) pre-mRNA is alternatively spliced in a tissue-specific manner, leading to the production of calcitonin mRNA containing exons 1-4 in thyroid C cells and CGRP mRNA containing exons 1-3, 5, and 6 in neurons. The calcitonin-specific fourth exon contains an exonic splice enhancer (ESE) that binds SRp55. We define the RNA binding site of SRp55 in the ESE and demonstrate that base changes that decrease the level of SRp55 binding decrease the level of calcitonin splicing in vitro and calcitonin mRNA production in vivo. Base changes that increase the affinity of SRp55 for the ESE increase the level of calcitonin splicing in vitro and calcitonin mRNA levels in 293 cells. We also observe that SRp55 levels in different cell types correlate with the levels of calcitonin mRNA produced in these cells. Finally, we show that increasing the level of cellular expression of SRp55 stimulates calcitonin mRNA production in vivo. These observations suggest that SRp55 binding to a suboptimal RNA binding site in the calcitonin/CGRP pre-mRNA ESE is required for calcitonin mRNA production. Differential amounts of SRp55 present in different cell types would then control calcitonin/CGRP alternative splicing.
可变剪接是调节基因表达的一种重要机制。哺乳动物降钙素/降钙素基因相关肽(CGRP)前体mRNA以组织特异性方式进行可变剪接,导致在甲状腺C细胞中产生包含外显子1-4的降钙素mRNA,在神经元中产生包含外显子1-3、5和6的CGRP mRNA。降钙素特异性的第四外显子包含一个与SRp55结合的外显子剪接增强子(ESE)。我们确定了SRp55在ESE中的RNA结合位点,并证明降低SRp55结合水平的碱基变化会降低体外降钙素剪接水平和体内降钙素mRNA的产生。增加SRp55与ESE亲和力的碱基变化会增加体外降钙素剪接水平和293细胞中降钙素mRNA水平。我们还观察到不同细胞类型中SRp55的水平与这些细胞中产生的降钙素mRNA水平相关。最后,我们表明增加SRp55的细胞表达水平会刺激体内降钙素mRNA的产生。这些观察结果表明,SRp55与降钙素/CGRP前体mRNA ESE中次优RNA结合位点的结合是降钙素mRNA产生所必需的。不同细胞类型中存在的不同量的SRp55将控制降钙素/CGRP的可变剪接。