Thermodynamic analyses of the constitutive splicing pathway for ovomucoid pre-mRNA

被引:2
作者
Ro-Choi, Tae Suk [1 ,2 ]
Choi, Yong Chun [1 ,2 ]
机构
[1] Baylor Coll Med, Dept Pharmacol, Houston, TX 77030 USA
[2] Dong A Univ, Med Res Ctr Canc Mol Therapy, Coll Med, Pusan 602714, South Korea
关键词
co-transcriptional folding; Mini-hairpins; snRNAs; U1; U2; U4; U5; U6; splicing; thermodynamics; GROUP-II INTRON; U1; SNRNA; 5'-SPLICE-SITE RECOGNITION; PRIMARY SEQUENCE; CHICKEN; SITE; SPLICEOSOME; ELEMENTS; BINDING; DUPLEX;
D O I
10.1007/s10059-009-0087-y
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The ovomucoid pre-mRNA has been folded into mini-hairpins adaptable for the RNA recognition motif (RRM) protein binding. The number of mini-hairpins were 372 for pre-mRNA and 83-86 for mature m RNA The spatial arrangements are, in average, 16 nucleotides per mini-hairpin which includes 7 nt in the stem, 5.6 nt in the loop and 3.7 nt in the inter-hairpin spacer. The constitutive splicing system of ovomucoid-pre-mRNA is characterized by preferred order of intron removal of 5/6 > 7/4 > 2/1 > 3. The 5' splice sites (5'SS), branch point sequences (BPS) and 3' splice sites (3'SS) were identified and free energies involved have been estimated in 7 splice sites. Thermodynamic barriers for splice sites from the least (| lowest | -Kcal) were 5,4, 7,6, 2,1, and 3; i.e., -18.7 Kcal, -20.2 Kcal, -21.0 Kcal, -24.0 Kcal, -25.4 Kcal, -26.4 Kcal and -28.2 Kcal respectively. These are parallel to the kinetic data of splicing order reported in the literature. As a result, the preferred order of intron removals can be described by a consideration of free energy changes involved in the spliceosomal assembly pathway. This finding is consistent with the validity of hnRNP formation mechanisms in previous reports.
引用
收藏
页码:657 / 665
页数:9
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