Warwick Medical School, University of Warwick, Gibbett Hill Road, Coventry CV4 7AL, United Kingdom.
J Biol Chem. 2010 Mar 12;285(11):7857-65. doi: 10.1074/jbc.M109.072892. Epub 2010 Jan 8.
The Drosophila melanogaster genome contains only one CPT1 gene (Jackson, V. N., Cameron, J. M., Zammit, V. A., and Price, N. T. (1999) Biochem. J. 341, 483-489). We have now extended our original observation to all insect genomes that have been sequenced, suggesting that a single CPT1 gene is a universal feature of insect genomes. We hypothesized that insects may be able to generate kinetically distinct variants by alternative splicing of their single CPT1 gene. Analysis of the insect genomes revealed that (a) the single CPT1 gene in each and every insect genome contains two alternative exons and (ii) in all cases, the putative alternative splicing site occurs within a small region corresponding to 21 amino acid residues that are known to be essential for the binding of substrates and of malonyl-CoA in mammalian CPT1A. We performed PCR analyses of mRNA from different Drosophila tissues; both of the anticipated splice variants of CPT1 mRNA were found to be expressed in all of the tissues tested (both in larvae and adults), with the expression level for one of the splice variants being significantly different between flight muscle and the fat body of adult Drosophila. Heterologous expression of the full-length cDNAs corresponding to the two putative variants of Drosophila CPT1 in the yeast Pichia pastoris revealed two important differences between the properties of the two variants: (i) their affinity (K(0.5)) for one of the substrates, palmitoyl-CoA, differed by 5-fold, and (ii) the sensitivity to inhibition by malonyl-CoA at fixed, higher palmitoyl-CoA concentrations was 2-fold different and associated with different kinetics of inhibition. These data indicate that alternative splicing that specifically affects a structurally crucial region of the protein is an important mechanism through which functional diversity of CPT1 kinetics is generated from the single gene that occurs in insects.
果蝇的基因组中只含有一个 CPT1 基因(Jackson,V. N.,Cameron,J. M.,Zammit,V. A.,and Price,N. T.(1999)Biochem. J. 341,483-489)。我们现在将最初的观察结果扩展到所有已测序的昆虫基因组,表明一个单一的 CPT1 基因是昆虫基因组的普遍特征。我们假设昆虫可能通过其单一的 CPT1 基因的选择性剪接产生动力学上不同的变体。对昆虫基因组的分析表明:(a)每个昆虫基因组中的单一 CPT1 基因包含两个选择性外显子;(ii)在所有情况下,推测的选择性剪接位点发生在一个小区域内,该区域对应于 21 个氨基酸残基,这些残基对于哺乳动物 CPT1A 中底物和丙二酰辅酶 A 的结合是必不可少的。我们对来自不同果蝇组织的 mRNA 进行了 PCR 分析;CPT1 mRNA 的两种预期剪接变体都在所有测试的组织中表达(幼虫和成虫),其中一种剪接变体的表达水平在果蝇的飞行肌和脂肪体之间有显著差异。与两种可能的变体相对应的全长 cDNA 在酵母毕赤酵母中的异源表达揭示了两种变体之间的两个重要区别:(i)它们对一种底物,棕榈酰辅酶 A 的亲和力(K0.5)不同 5 倍;(ii)在固定的较高棕榈酰辅酶 A 浓度下,对丙二酰辅酶 A 的抑制敏感性不同 2 倍,并且与抑制的不同动力学相关。这些数据表明,特异性影响蛋白质结构关键区域的选择性剪接是一种重要的机制,通过该机制,昆虫中存在的单一基因产生 CPT1 动力学的功能多样性。