Tran Trung T, Bollineni Ravi C, Strozynski Margarita, Koehler Christian J, Thiede Bernd
Department of Biosciences, University of Oslo , Oslo 0316, Norway.
J Proteome Res. 2017 Jul 7;16(7):2571-2578. doi: 10.1021/acs.jproteome.7b00126. Epub 2017 May 25.
Alternative splicing is a mechanism in eukaryotes by which different forms of mRNAs are generated from the same gene. Identification of alternative splice variants requires the identification of peptides specific for alternative splice forms. For this purpose, we generated a human database that contains only unique tryptic peptides specific for alternative splice forms from Swiss-Prot entries. Using this database allows an easy access to splice variant-specific peptide sequences that match to MS data. Furthermore, we combined this database without alternative splice variant-1-specific peptides with human Swiss-Prot. This combined database can be used as a general database for searching of LC-MS data. LC-MS data derived from in-solution digests of two different cell lines (LNCaP, HeLa) and phosphoproteomics studies were analyzed using these two databases. Several nonalternative splice variant-1-specific peptides were found in both cell lines, and some of them seemed to be cell-line-specific. Control and apoptotic phosphoproteomes from Jurkat T cells revealed several nonalternative splice variant-1-specific peptides, and some of them showed clear quantitative differences between the two states.
可变剪接是真核生物中的一种机制,通过该机制可从同一基因产生不同形式的mRNA。可变剪接变体的鉴定需要鉴定特定于可变剪接形式的肽段。为此,我们构建了一个人类数据库,该数据库仅包含来自Swiss-Prot条目的、特定于可变剪接形式的独特胰蛋白酶肽段。使用该数据库能够轻松获取与质谱数据匹配的、特定于剪接变体的肽段序列。此外,我们将这个不包含可变剪接变体1特异性肽段的数据库与人类Swiss-Prot数据库进行了合并。这个合并后的数据库可作为用于搜索液相色谱-质谱数据的通用数据库。使用这两个数据库对源自两种不同细胞系(LNCaP、HeLa)的溶液内消化产物的液相色谱-质谱数据以及磷酸化蛋白质组学研究进行了分析。在这两种细胞系中均发现了几种非可变剪接变体1特异性肽段,其中一些似乎具有细胞系特异性。来自Jurkat T细胞的对照和凋亡磷酸化蛋白质组揭示了几种非可变剪接变体1特异性肽段,其中一些在两种状态之间表现出明显的定量差异。