Matches in SemOpenAlex for { <https://semopenalex.org/work/W2111438274> ?p ?o ?g. }
- W2111438274 abstract "Abstract Background Mammalian antimicrobial peptides (AMPs) are effectors of the innate immune response. A multitude of signals coming from pathways of mammalian pathogen/pattern recognition receptors and other proteins affect the expression of AMP-coding genes (AMPcgs). For many AMPcgs the promoter elements and transcription factors that control their tissue cell-specific expression have yet to be fully identified and characterized. Results Based upon the RIKEN full-length cDNA and public sequence data derived from human, mouse and rat, we identified 178 candidate AMP transcripts derived from 61 genes belonging to 29 AMP families. However, only for 31 mouse genes belonging to 22 AMP families we were able to determine true orthologous relationships with 30 human and 15 rat sequences. We screened the promoter regions of AMPcgs in the three species for motifs by an ab initio motif finding method and analyzed the derived promoter characteristics. Promoter models were developed for alpha-defensins, penk and zap AMP families. The results suggest a core set of transcription factors (TFs) that regulate the transcription of AMPcg families in mouse, rat and human. The three most frequent core TFs groups include liver-, nervous system-specific and nuclear hormone receptors (NHRs). Out of 440 motifs analyzed, we found that three represent potentially novel TF-binding motifs enriched in promoters of AMPcgs, while the other four motifs appear to be species-specific. Conclusion Our large-scale computational analysis of promoters of 22 families of AMPcgs across three mammalian species suggests that their key transcriptional regulators are likely to be TFs of the liver-, nervous system-specific and NHR groups. The computationally inferred promoter elements and potential TF binding motifs provide a rich resource for targeted experimental validation of TF binding and signaling studies that aim at the regulation of mouse, rat or human AMPcgs." @default.
- W2111438274 created "2016-06-24" @default.
- W2111438274 creator A5015583721 @default.
- W2111438274 creator A5028835404 @default.
- W2111438274 creator A5030167983 @default.
- W2111438274 creator A5032097008 @default.
- W2111438274 creator A5038912417 @default.
- W2111438274 creator A5040448365 @default.
- W2111438274 creator A5044306593 @default.
- W2111438274 creator A5055569646 @default.
- W2111438274 creator A5062430868 @default.
- W2111438274 creator A5068559343 @default.
- W2111438274 creator A5072131150 @default.
- W2111438274 creator A5082267036 @default.
- W2111438274 creator A5084679761 @default.
- W2111438274 creator A5086500057 @default.
- W2111438274 date "2006-12-01" @default.
- W2111438274 modified "2023-10-17" @default.
- W2111438274 title "Computational promoter analysis of mouse, rat and human antimicrobial peptide-coding genes" @default.
- W2111438274 cites W105427898 @default.
- W2111438274 cites W148852109 @default.
- W2111438274 cites W1503306485 @default.
- W2111438274 cites W1516030996 @default.
- W2111438274 cites W1549934738 @default.
- W2111438274 cites W1784478130 @default.
- W2111438274 cites W1839029331 @default.
- W2111438274 cites W1843241178 @default.
- W2111438274 cites W1918776755 @default.
- W2111438274 cites W1963891653 @default.
- W2111438274 cites W1964234893 @default.
- W2111438274 cites W1987067683 @default.
- W2111438274 cites W1994640266 @default.
- W2111438274 cites W1996790111 @default.
- W2111438274 cites W2008508452 @default.
- W2111438274 cites W2015770408 @default.
- W2111438274 cites W2016912110 @default.
- W2111438274 cites W2025063713 @default.
- W2111438274 cites W2025289680 @default.
- W2111438274 cites W2026028158 @default.
- W2111438274 cites W2031772919 @default.
- W2111438274 cites W2033538734 @default.
- W2111438274 cites W2042611635 @default.
- W2111438274 cites W2043928258 @default.
- W2111438274 cites W2046844678 @default.
- W2111438274 cites W2047710219 @default.
- W2111438274 cites W2054457667 @default.
- W2111438274 cites W2055043387 @default.
- W2111438274 cites W2058682865 @default.
- W2111438274 cites W2060306551 @default.
- W2111438274 cites W2082440796 @default.
- W2111438274 cites W2085977869 @default.
- W2111438274 cites W2088255739 @default.
- W2111438274 cites W2088304498 @default.
- W2111438274 cites W2090215742 @default.
- W2111438274 cites W2095351093 @default.
- W2111438274 cites W2096525273 @default.
- W2111438274 cites W2097045992 @default.
- W2111438274 cites W2099275700 @default.
- W2111438274 cites W2099468911 @default.
- W2111438274 cites W2106449126 @default.
- W2111438274 cites W2107580398 @default.
- W2111438274 cites W2108774839 @default.
- W2111438274 cites W2112946930 @default.
- W2111438274 cites W2125012054 @default.
- W2111438274 cites W2130933726 @default.
- W2111438274 cites W2131958110 @default.
- W2111438274 cites W2135030836 @default.
- W2111438274 cites W2141408320 @default.
- W2111438274 cites W2145091349 @default.
- W2111438274 cites W2151080095 @default.
- W2111438274 cites W2160780417 @default.
- W2111438274 cites W2161732139 @default.
- W2111438274 cites W2164296513 @default.
- W2111438274 cites W2167499479 @default.
- W2111438274 cites W2170912840 @default.
- W2111438274 cites W2189513341 @default.
- W2111438274 cites W2400961152 @default.
- W2111438274 cites W2469080257 @default.
- W2111438274 cites W2495184785 @default.
- W2111438274 cites W4213060373 @default.
- W2111438274 cites W4236324471 @default.
- W2111438274 cites W4248318091 @default.
- W2111438274 cites W1973340890 @default.
- W2111438274 doi "https://doi.org/10.1186/1471-2105-7-s5-s8" @default.
- W2111438274 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/1764486" @default.
- W2111438274 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/17254313" @default.
- W2111438274 hasPublicationYear "2006" @default.
- W2111438274 type Work @default.
- W2111438274 sameAs 2111438274 @default.
- W2111438274 citedByCount "28" @default.
- W2111438274 countsByYear W21114382742012 @default.
- W2111438274 countsByYear W21114382742013 @default.
- W2111438274 countsByYear W21114382742015 @default.
- W2111438274 countsByYear W21114382742016 @default.
- W2111438274 countsByYear W21114382742017 @default.
- W2111438274 countsByYear W21114382742018 @default.
- W2111438274 countsByYear W21114382742020 @default.
- W2111438274 crossrefType "journal-article" @default.
- W2111438274 hasAuthorship W2111438274A5015583721 @default.
- W2111438274 hasAuthorship W2111438274A5028835404 @default.