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PolyA_DB: a database for mammalian mRNA polyadenylation
Haibo Zhang1, Jun Hu, Michael Recce
1Center for Computational Biology and Bioengineering, New Jersey Institute of Technology, Newark, NJ 07102, USA.
Abstract:
Messenger RNA polyadenylation is one of the key post-transcriptional events in eukaryotic cells. A large number of genes in mammalian species can undergo alternative polyadenylation, which leads to mRNAs with variable 3' ends. As the 3' end of mRNAs often contains cis elements important for mRNA stability, mRNA localization and translation, the implications of the regulation of polyadenylation can be multifold. Alternative polyadenylation is controlled by cis elements and trans factors, and is believed to occur in a tissue- or disease-specific manner. Given the availability of many databases devoted to other aspects of mRNA metabolism, such as transcriptional initiation and splicing, systematic information on polyadenylation, including alternative polyadenylation and its regulation, is noticeably lacking. Here, we present a database named polyA_DB, through which we strive to provide several types of information regarding polyadenylation in mammalian species: (i) polyadenylation sites and their locations with respect to the genomic structure of genes; (ii) cis elements surrounding polyadenylation sites; (iii) comparison of polyadenylation configuration between orthologous genes; and (iv) tissue/organ information for alternative polyadenylation sites. Currently, polyA_DB contains 45,565 polyadenylation sites for 25,097 human and mouse genes, representing the most comprehensive polyadenylation database till date. The database is accessible via the website (http://polya.umdnj.edu/polyadb).
Insights
Messenger RNA polyadenylation is crucial for gene expression. The new polyA_DB database offers comprehensive data on mammalian polyadenylation sites and regulation, filling a critical gap for researchers.
Area of Science:
- Molecular Biology
- Genomics
- Bioinformatics
Background:
- Messenger RNA (mRNA) polyadenylation is a critical post-transcriptional regulatory mechanism in eukaryotic gene expression.
- Alternative polyadenylation (APA) generates mRNA variants with different 3' ends, impacting mRNA stability, localization, and translation.
- Existing biological databases lack systematic, comprehensive information on polyadenylation and APA.
Purpose of the Study:
- To establish polyA_DB, a centralized database for mammalian polyadenylation information.
- To provide detailed data on polyadenylation sites, associated cis-elements, and APA regulation.
- To facilitate research on mRNA metabolism and its implications in various biological contexts.
Main Methods:
- Compilation of polyadenylation site data from human and mouse genes.
- Annotation of genomic locations and surrounding cis-regulatory elements for each polyadenylation site.
- Inclusion of comparative data for orthologous genes and tissue-specific APA information.
Main Results:
- The polyA_DB database currently houses 45,565 polyadenylation sites for 25,097 human and mouse genes.
- It provides comprehensive information on polyadenylation sites, cis-elements, orthologous gene comparisons, and tissue-specific APA.
- Represents the most extensive collection of polyadenylation data available to date.
Conclusions:
- The polyA_DB database significantly enhances the accessibility of crucial information on mRNA polyadenylation and APA.
- It serves as a valuable resource for studying gene regulation, mRNA processing, and disease mechanisms.
- Facilitates future research by providing a unified platform for polyadenylation-related data analysis.
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