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. 2018 Jun 27;8:9759. doi: 10.1038/s41598-018-28094-6

Table 1.

Description of NAT gene constructs and their primate species of origin.

Scientific name (synonym)a Common namea Taxon mnemonica Taxon IDa Geneb GenBank IDb Amplification primersc
Allenopithecus nigroviridis Allen’s swamp monkey ALLNI 54135 NAT1 KU640972 #1 and #2
Cercopithecus diana Diana monkey CERDI 36224 NAT1 KU640973 #1 and #2
NAT2 KU640982 #1 and #3
Chlorocebus tantalus (Cercopithecus tantalus) Tantalus monkey CHLTN 60712 NAT1 KU640974 #6 and #7
NAT2 KU640983 #1 and #3
Erythrocebus patas (Cercopithecus patas) Red guenon ERYPA 9538 NAT1 KU640975 #6 and #7
NAT2 KU640984 #1 and #3
Homo sapiens Human HUMAN 9606 NAT1 X17059 (allele NAT1*4) #1 and #2
NAT2 X14672 (allele NAT2*4) Clone available
Macaca mulatta Rhesus macaque MACMU 9544 NAT1 KU640969 #1 and #2
NAT2 AJ504440 (allele NAT2*1) Clone available
Macaca sylvanus Barbary macaque MACSY 9546 NAT1 KU640970 #1 and #2
NAT2 KU640978 #1 and #3
Mandrillus sphinx (Papio sphinx) Mandrill MANSP 9561 NAT1 KU640971 #1 and #2
NAT2 KU640980 #1 and #3
Nomascus gabriellae Red-cheeked gibbon NOMGA 61852 NAT1 KU640967 #1 and #2
NAT2 KU640985 #1 and #4
Sapajus paella (Cebus apella) Brown-capped capuchin SAPAP 9515 NAT1 KU640966 #1 and #2
Trachypithecus cristatus (Presbytis cristata) Silvered leaf-monkey TRACR 122765 NAT1 KU640968 #1 and #2
NAT2 KU640977 #1 and #5

aThe current scientific names of species with synonymous names in parentheses (first column) and a common name (second column), are from the UniProt Taxonomy database (http://www.uniprot.org/taxonomy/). Official taxon mnemonics (third column) and taxon identification numbers (fourth column) are from the same source. According to current consensus nomenclature (http://nat.mbg.duth.gr/), taxon mnemonics are attached to the symbols of NAT genes to identify their specific organism of origin22.

bAll NAT gene annotations (fifth column) are as first described by6, except for the NAT2 gene of M. mulatta60, and the NAT1 and NAT2 genes of H. sapiens66. The recombinant proteins expressed in this study were as predicted by translation of the nucleotide sequences for which GenBank identification numbers are provided (sixth column).

cThe complete coding sequence of each NAT gene was amplified for cloning, using combinations of the following primers, as indicated (seventh column): Primer #1 (forward), GCGGCAGCCATATGGACATTGAAGCATA; Primer #2 (reverse), TCGAGTGCGGCCGCCTAAATAGTAAAAAATCTATCACC; Primer #3 (reverse), GTGCTCGAGTGCGGCCGCCTAAATAGTGAAGGATC; Primer #4 (reverse), TCGAGTGCGGCCGCCTAAATAGTAAGGGATCCATC; Primer #5 (reverse), TCGAGTGCGGCCGCCTAAATAGTAAAGAATCCATC. The recognition sites for restriction endonucleases NdeI (forward primer) and NotI (reverse primers) are underlined. Clones for the NAT2 genes of M. mulatta and H. sapiens were available in our laboratories from previous studies61. The NAT1 constructs of C. tantalus and E. patas were generated from the NAT1 construct of C. diana via site-directed mutagenesis with Primer #6 (forward), CCATGGACTTAGGCTTAGAGGCCAT, and Primer #7 (reverse), ATGGCCTCTAAGCCTAAGTCCATGG (in bold, the mutagenised nucleotide representing the only non-synonymous SNP differentiating the NAT1 gene of C. diana from the other two homologues). Amplification of the NAT2 genes of A. nigroviridis (GenBank ID: KU640981) and S. apella (GeneBank ID: KU640976) was not possible due to limited availability of genomic DNA.