Study / S02YIX2JW2019-10-24
Influence of genetic polymorphism on transcriptional enhancer activity in the malaria vector Anopheles coluzzii
Luisa Nardini, Inge Holm, Adrien Pain, Emmanuel Bischoff, Daryl M. Gohl et al.
About this study
Enhancers are cis-regulatory elements that control most of the developmental and spatial gene expression in eukaryotes. Genetic variation of enhancer sequences is known to influence phenotypes, but the effect of enhancer variation upon enhancer functional activity and downstream phenotypes has barely been examined in any species. In the African malaria vector, Anopheles coluzzii, we identified candidate enhancers in the proximity of genes relevant for immunity, insecticide resistance, and development. The candidate enhancers were functionally validated using luciferase reporter assays, and their activity was found to be essentially independent of their physical orientation, a typical property of enhancers. All of the enhancers segregated genetically polymorphic alleles, which displayed significantly different levels of functional activity. Deletion mutagenesis and functional testing revealed a fine structure of positive and negative regulatory elements that modulate activity of the enhancer core. Enhancer polymorphisms segregate in wild A. coluzzii populations in West Africa. Thus, enhancer variants that modify target gene expression leading to likely phenotypic consequences are frequent in nature. These results demonstrate the existence of naturally polymorphic A. coluzzii enhancers, which may help explain important differences between individuals or populations for malaria transmission efficiency and vector adaptation to the environment.
Full author list & citation
Luisa Nardini, Inge Holm, Adrien Pain, Emmanuel Bischoff, Daryl M. Gohl, Soumanaba Zongo, Wamdaogo M. Guelbeogo, N’Fale Sagnon, Kenneth D. Vernick, Michelle M. Riehle. Influence of genetic polymorphism on transcriptional enhancer activity in the malaria vector Anopheles coluzzii. 2019-10-24. https://doi.org/10.1038/s41598-019-51730-8
Experiments 5
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Two natural LRIM1 alleles were shortened symmetrically from both ends to produce 100%, 50%, and 25% derivatives, then tested in the same episomal dual-luciferase reporter system. The panel resolves allele-specific positive and negative regulatory modules within the LRIM1 interval.
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A pooled genomic-fragment STARR-seq library from 60 wild A. coluzzii was transfected into A. coluzzii 4a3A cells in three biological replicates. Candidate enhancers were selected near six vector-biology genes where reporter cDNA coverage visibly exceeded the plasmid-DNA baseline.
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Each candidate interval was cloned into an episomal pGL-Gateway-DSCP firefly-luciferase reporter and co-transfected with pRL-ubi-63E Renilla control in A. coluzzii 4a3A cells. Activity was normalized to the DLX negative-control construct.
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Selected KLF, AP, and LRIM1 enhancer alleles were recloned in both arbitrary reporter orientations and assayed in A. coluzzii 4a3A cells. The source reports no detectable orientation effect for KLF/AP and a weak LRIM1 Fd05_#1 difference.
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Naturally segregating enhancer haplotypes amplified from Ngousso and Fd colonies were cloned into pGL-Gateway-DSCP and assayed for allele-dependent enhancer activity in A. coluzzii 4a3A cells. The panel covers six validated enhancer loci and includes the sequence of each tested allele from Supplementary File S1.