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Methods to Discover Alternative Promoter Usage and Transcriptional Regulation of Murine Bcrp1
Published on: May 27, 2016
Characterization and Analysis of Mammalian AKR7A Gene Promoters: Implications for Transcriptional Regulation
Samiul Alam Rajib1, Mohammad Kawsar Sharif Siam2,3
1Department of Pharmacy, Brac University, 41, Pacific Tower, Mohakhali, Dhaka, 1212, Bangladesh. s.a.rajib@bracu.ac.bd.
Abstract:
Aldo-keto reductase (AKR) superfamily is responsible for preventing mammalian cells from the toxic and carcinogenic effect of different genotoxic and non-genotoxic chemicals by reducing them, though the inducibility of these genes are different in different species. The aim of this paper is to compare the gene regulation mechanisms of AKR superfamily genes in different species and to identify the conserved areas, which are responsible for gene regulations in the presence of antioxidant, toxicants, and non-genotoxic carcinogens. At the beginning of the analysis AKR genes found in different species were divided into two groups based on their amino acid sequence similarities. Comparison of AKR7A gene clusters between different species revealed that Human AKR7A2 has orthologues in mammalians like rat, mouse, pigs, and other primates. On the other hand, AKR7A3 has orthologues only in rat and AKR7L is present only in primates. All the genes of AKR superfamily have a trend to stay in clusters in mammalian chromosomes having repeated sequences in between them. Transcription start site analysis revealed that genes like human AKR7A2 and rat Akr7a4 do not have conventional promoter regions such as TATA box, CAAT box and have several GC-rich regions, whereas gene like Akr7a1 contains a TATA box 25 bp upstream of transcription start site instead of having CpG islands. Putative orthologous genes i.e., rat AKR7A4, human AKR7A2, and mouse AKR7A5 share more common features such as common transcription factor binding site for specificity protein 1 (SP1), GATA binding factor family, Selenocysteine tRNA gene transcription activating factor (STAF) zinc finger protein, Krüppel-like C2H2 zinc finger (HICF) protein, negative glucocorticoid response element (NGRE) etc. Similarly, genes like rat AKR7A1, human AKR7A3, and human AKR7L share common sequence and transcription factor binding sites. Among those, Nuclear factor erythroid 2-related factor 2 (Nrf2) is thought to be responsible for the inducibility of these genes in the presence of antioxidants. Our analysis revealed that AKR7A gene family consists of genes having a large number of variations in them. Some of these, such as AKR7A2 are housekeeping genes, on the other hand, genes like AKR7A3 are highly inducible in the presence of antioxidants because of the presence of Nrf2 binding site in their promoter. AKR7A1 has a different promoter than others and function of AKR7L gene is still unknown.
Insights
The Aldo-keto reductase (AKR) superfamily protects cells from toxic chemicals. Gene regulation varies by species, with some AKR genes inducible by antioxidants via Nrf2 binding sites.
Area of Science:
- Biochemistry
- Genetics
- Toxicology
Background:
- The Aldo-keto reductase (AKR) superfamily detoxifies mammalian cells from harmful chemicals.
- Gene inducibility within the AKR superfamily differs across species.
- Understanding AKR gene regulation is crucial for predicting cellular responses to toxicants and carcinogens.
Purpose of the Study:
- To compare AKR superfamily gene regulation mechanisms across different species.
- To identify conserved regulatory regions involved in responses to antioxidants, toxicants, and carcinogens.
- To elucidate the evolutionary and functional diversity within the AKR7A gene family.
Main Methods:
- Bioinformatic analysis of AKR gene clusters and amino acid sequence similarities.
- Transcription start site analysis to identify promoter elements (e.g., TATA box, GC-rich regions).
- Comparative analysis of transcription factor binding sites in orthologous genes.
Main Results:
- AKR7A genes exhibit species-specific ortholog distribution (e.g., Human AKR7A2 in primates and rodents, AKR7A3 in rats, AKR7L in primates).
- AKR genes cluster on mammalian chromosomes with interspersed repeats.
- Orthologous genes like human AKR7A2 and rat AKR7A4 share common transcription factor binding sites (SP1, GATA, STAF, HICF, NGRE).
- The Nuclear factor erythroid 2-related factor 2 (Nrf2) binding site is associated with antioxidant inducibility in genes like AKR7A3.
- AKR7A2 functions as a housekeeping gene, while AKR7A3 is highly inducible.
Conclusions:
- The AKR7A gene family displays significant variation in regulatory mechanisms and functions.
- Conserved transcription factor binding sites, particularly Nrf2, play a key role in AKR gene inducibility by antioxidants.
- Species-specific differences in AKR gene promoters and functions, such as the housekeeping role of AKR7A2 and the inducibility of AKR7A3, highlight evolutionary adaptations.
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