Abstract
Serial Analysis of Gene Expression (SAGE) and Massively Parallel Signature Sequencing (MPSS) are powerful techniques for gene expression analysis. A crucial step in analyzing SAGE and MPSS data is the assignment of experimentally obtained tags to a known transcript. However, tag to transcript assignment is not a straightforward process since alternative tags for a given transcript can also be experimentally obtained. Here, we have evaluated the impact of Single Nucleotide Polymorphisms (SNPs) on the generation of alternative SAGE and MPSS tags. This was achieved through the construction of a reference database of SNP-associated alternative tags, which has been integrated with SAGE Genie. A total of 2020 SNP-associated alternative tags were catalogued in our reference database and at least one SNP-associated alternative tag was observed for approximately 8.6% of all known human genes. A significant fraction (61.9%) of these alternative tags matched a list of experimentally obtained tags, validating their existence. In addition, the origin of four out of five SNP-associated alternative MPSS tags was experimentally confirmed through the use of the GLGI-MPSS protocol (Generation of Long cDNA fragments for Gene Identification). The availability of our SNP-associated alternative tag database will certainly improve the interpretation of SAGE and MPSS experiments.
MeSH Terms
DNA Restriction Enzymes/metabolism
Databases, Genetic
Gene Expression Profiling/methods
Humans
Molecular Sequence Data
Polymorphism, Single Nucleotide
RNA, Messenger/chemistry
Sequence Analysis, RNA
Sequence Tagged Sites
Chemicals
RNA, Messenger
DNA Restriction Enzymes
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Silva Ana Paula M
Laboratory of Molecular Biology, Ludwig Institute for Cancer Research, 01509-010, São Paulo, SP, Brazil.
De Souza Jorge E S
Galante Pedro A F
Riggins Gregory J
De Souza Sandro J
Camargo Anamaria A
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