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Mutational Analysis of N-Ethyl-N-Nitrosourea (ENU) In bioRxiv preprint doi: https://doi.org/10.1101/486266; this version posted December 3, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. 1 Mutational analysis of N-ethyl-N-nitrosourea (ENU) in 2 the fission yeast Schizosaccharomyces pombe. 3 Rafael Hoyos-Manchado1, Juan Jiménez1* and Víctor A. Tallada1* 4 1Centro Andaluz de Biología del Desarrollo, Universidad Pablo de Olavide/Consejo 5 Superior de Investigaciones Científicas, Carretera de Utrera Km1, 41013 Seville, Spain. 6 *Corresponding authors 7 E-mail: [email protected] 8 9 10 11 12 13 14 15 16 17 1 bioRxiv preprint doi: https://doi.org/10.1101/486266; this version posted December 3, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. 18 Abstract 19 Forward genetics has boosted our knowledge on genic function in a multitude of 20 biological models and it has significantly contributed to the understanding of genetic 21 bases of development, ageing and human diseases. With the advent of the next 22 generation sequencing and use of powerful bioinformatic tools, this traditional genetic 23 strategy has acquired a new impulse. At present, whole genome sequencing assisted by 24 in silico analysis allows the rapid and efficient identification of gene variants that are 25 responsible for a particular phenotype. In this experimental pipeline, it is crucial to start 26 by provoking a large number of random changes in the genome of the model organisms 27 to be screened. A range of chemical mutagens are used to this end because most of them 28 display particular reactivity properties and act differently over DNA. Here we use N- 29 ethyl-N-nitrosourea (ENU) as a mutagen for the first time to our knowledge in the 30 fission yeast Schizosaccharomyces pombe. By comparison to the extensively used Ethyl 31 methanesulfonate (EMS) in a phenotype-based study, we conclude that ENU is a very 32 potent and easy-to-use mutagen. Judging from DNA sequence analysis of the identified 33 mutants, ENU induces base changes rather than indels and the mutational spectrum in 34 the fission yeast seems similar to that found in mice but different to that described in 35 other single-celled organisms such as budding yeast and E. coli. Using ENU in S. 36 pombe, we have gathered a collection of 49 auxotrophic mutants including two 37 deleterious alleles of ATIC human ortholog. Defective alleles of this gene are causative 38 of AICA-Ribosiduria, a severe genetic disease. We have also identified 5 39 aminoglycoside-resistance inactivating mutations in APH genes. All these mutations 40 reported here may be of interest in the metabolism and antibiotic resistance research 41 fields. 2 bioRxiv preprint doi: https://doi.org/10.1101/486266; this version posted December 3, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. 42 Introduction 43 The search of a particular phenotype of interest after natural or induced random 44 mutation in biological models, and the consequent identification of the underlying 45 genetic variant, is known as forward genetics. This strategy provides an extremely 46 powerful tool to characterise individual gene functions as well as complex genetic 47 pathways interplay, when two or more mutations coexist into the same cell. Human 48 genetic diseases are usually provoked by hypomorphic mutations (partial loss of 49 function) that allow embryo development and birth but become deleterious at later 50 stages. Therefore, by inducing DNA changes into model organisms, genetic bases of 51 human diseases can be very closely reproduced to be studied; even in single-celled 52 organisms such as yeast [1]. 53 A number of physical and chemical mutagens have been used to boost the 54 number of random changes over the natural spontaneous mutation rate. In addition to 55 single base substitutions, most of these agents also provoke small insertions and 56 deletions (generically known as indels) [2]. Indels usually lead to frame shifts that 57 generate either truncated or aberrant polypeptides. These provide very valuable 58 information on non-essential gene functions because very often abolish the 59 corresponding protein function entirely or disrupt complexes where they work in, 60 mimicking the full gene deletion phenotype. However, the ideal genetic variants to 61 study essential genes consist of mutations that enable an “on-off” function switch under 62 given conditions. So called conditional alleles are very often generated by individual 63 amino acid substitutions which “chirurgeonly” destroy postraductional modification 64 sites, unwind binding motives, impair the active centre, etc. without dramatically 65 affecting the overall polypeptide´s structure and/or complexes they are part of. For 3 bioRxiv preprint doi: https://doi.org/10.1101/486266; this version posted December 3, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. 66 theses alleles, the switch to destroy function, activity or structure when desired can be 67 turned off simply modulating the culture conditions (temperature, media, presence of 68 chemicals, etc.) [3-5]. These mutations enable elegant genetic studies -otherwise 69 impossible- of essential genes applied to structure-function relationships, biochemical 70 regulation, protein-protein and protein to other partners interactions, etc. Therefore, 71 depending on the aim of the study, it would be desirable to use specific mutagens to 72 enrich the screens for single point substitutions. 73 Ethyl methanesulfonate (EMS), N-Methyl-N′-nitro-N-nitrosoguanidine 74 (MNNG) and Methyl methanesulfonate (MMS) are within the most common alkylating 75 agents used in yeast and other model organisms as mutation inducing agents [4, 6-8]. 76 Another alkylating agent, N-ethyl-N-nitrosourea (ENU), has also been extensively used 77 for a long time for random mutagenesis screens, especially in mice [9]. However, as far 78 as we know, we are the only ones to use it as a mutagen in fission yeast [3]. As other 79 alkylating counterparts, ENU does not need to be metabolised to alkylate DNA 80 proactively in vivo [10-12]. Resulting ethylated nucleotides are mispaired, leading to 81 base pair substitutions after two replication rounds. Importantly, the chemical reactivity 82 described for this molecule remarkably differs from EMS and MMS in the Swain-Scott 83 substrate constant [13, 14]. An especially attractive feature of this molecule is that 84 Indels are extremely rare in its mutagenic repertoire [15, 16]; We report here the use of 85 N-ethyl-N-nitrosourea (ENU) as an effective mutagen in the model yeast 86 Schizosaccharomyces pombe which may significantly enrich the isolation of new 87 single-base mutant alleles. 88 4 bioRxiv preprint doi: https://doi.org/10.1101/486266; this version posted December 3, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. 89 Materials and methods 90 Media and growth conditions 91 Standard fission yeast growth media and molecular biology approaches were used 92 throughout [17]. For qualitative spot tests to assess auxotrophy, every candidate strain 93 was inoculated from a plate in a unique well of a 96-well plate in YES liquid media. 94 After 13 hours, they were diluted 10-fold and plated onto YES and supplemented 95 minimal media lacking adenine, uridine, histidine or leucine in each case. Sporulation 96 agar (SPA) was used for mating and sporulation. Tetrad pulling for segregation analyses 97 was performed in a Singer MSM 400 automated dissection microscope (Singer 98 Instruments). 99 Mutagenesis 100 A reference strain, bearing G418 and Hygromycin B resistance markers integrated into 101 chromosome I and II respectively, was mutagenized using N-ethyl-N-nitrosourea (ENU; 102 Sigma N3385) or ethyl methanesulfonate (EMS; Sigma M0880) as in Winston, 2008 103 with minor variations [18]. Cells were grown overnight to mid log phase in 500 ml YES 104 medium at 30°C. Cells were concentrated to 2·108 cells/ml and 2 ml aliquots were 105 washed twice with 2 ml of water (centrifuge 5-10 seconds maximum speed), 106 resuspended in 7 ml 0.1 M sodium phosphate buffer (pH 7.0) and split into four 107 aliquots. One of them was treated with 50 ul EMS (0.3 M final) for 1 hour at 30ºC, and 108 another one was treated with 60 μl ENU (0.03 M final) for 20 minutes at 30ºC. The 109 other two were not treated with mutagens to be used as controls. For ENU treatment and 110 its control, 0.2 ml of each were taken and washed three times with Minimal Medium 5 bioRxiv preprint doi: https://doi.org/10.1101/486266; this version posted December 3, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license.
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