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This work explains how to transform yeast mitochondria using a biolistic method. We also show how to select and purify the transformants and how to introduce the desired mutation in the target position within the mitochondrial genome.
Baker´s yeast Saccharomyces cerevisiae has been widely used to understand mitochondrial biology for decades. This model has provided knowledge about essential, conserved mitochondrial pathways among eukaryotes, and fungi or yeast-specific pathways. One of the many abilities of S. cerevisiae is the capacity to manipulate the mitochondrial genome, which so far is only possible in S. cerevisiae and the unicellular algae Chlamydomonas reinhardtii. The biolistic transformation of yeast mitochondria allows us to introduce site-directed mutations, make gene rearrangements, and introduce reporters. These approaches are mainly used to understand the mechanisms of two highly coordinated processes in mitochondria: translation by mitoribosomes and assembly of respiratory complexes and ATP synthase. However, mitochondrial transformation can potentially be used to study other pathways. In the present work, we show how to transform yeast mitochondria by high-velocity microprojectile bombardment, select and purify the intended transformant, and introduce the desired mutation in the mitochondrial genome.
The yeast Saccharomyces cerevisiae is a widely recognized model used to study mitochondrial biogenesis. Since yeast is an anaerobic, facultative organism, it is possible to extensively study the causes and consequences of introducing mutations that impair respiration. In addition, this organism possesses friendly genetic and biochemical tools to study mitochondrial pathways. However, one of the most powerful resources to explore the mechanisms of respiratory complex assembly and mitochondrial protein synthesis is the ability to transform mitochondria and modify the organelle's genome. Previously, it has been helpful to introduce in the mitochondrial DNA (....
NOTE: We recommend making six transformations for each construct since mitochondrial transformation efficiency is usually low. The composition of the different growth media is shown in Table 2.
1. Tungsten particle preparation
This section presents some representative results from the different stages of mitochondrial transformation. Figure 6 shows a bombardment procedure. The synthetic rho- cells carried a bacterial plasmid with the reporter gene ARG8m, which will replace the coding sequence of a mitochondrial gene (Figure 6A). After bombardment, the plate was replicated on a medium lacking uracil (-URA); this is the master plate (
The present work described how to transform mitochondria from the yeast S. cerevisiae successfully. The process, from high-velocity microprojectile bombardment until purification of the intended yeast strain, takes ~8-12 weeks, depending on how many rounds of purification of the synthetic rho- strain are necessary. Some of the critical steps of the method are as follows. First, the larger the flanking regions added around the mutation site in the mitochondrial gene construct, the higher the probabilit.......
This publication was supported by Programa de Apoyo a Proyectos de Investigación e Innovación Tecnológica (PAPIIT), UNAM [IN223623 to XP-M]. UPD is a CONAHCYT fellow (CVU:883299). We want to thank Dr. Ariann Mendoza-Martínez for technical help with the light microscope images. Biorender licenses: DU26OMVLUU (Figure 2); BK26TH9GXH (Figure 3); GD26TH80R5 (Figure 4); PU26THARYD (Figure 7); ML26THAIFG (Figure 9).
....Name | Company | Catalog Number | Comments |
1 mL pipette tips | Axygen | T-1000-B | |
1.5 mL Microtube | Axygen | MCT-150-C | |
10 μL pipette tips | Axygen | T-10-C | |
15 mL conical bottom tube | Axygen | SCT-25ML-25-S | |
200 μL pipette tips | Axygen | T-200-Y | |
50 mL conical bottom tube | Axygen | SCT-50ML-25-S | |
AfiII | New England BioLabs | R0520S | |
Agarose | SeaKem | 50004 | |
Analytic balance | OHAUS | ARA520 | |
Autoclave | TOMY | ES-315 | |
Bacto agar | BD | 214010 | |
Bacto peptone | BD | 211677 | |
Biolisitic Macrocarrier holder | BIO-RAD | 1652322 | |
Bunsen burner | VWR | 89038-528 | |
Calcium chloride | Fisher Scientific | C79-500 | |
CSM -ADE | Formedium | DCS0049 | |
CSM -ARG | Formedium | DCS0059 | |
CSM -LEU | Formedium | DCS0099 | |
CSM -URA | Formedium | DCS0169 | |
Culture glass flask | KIMAX KIMBLE | 25615 | |
Culture glass tube | Pyrex | 9820 | |
Dextrose | BD | 215520 | |
Ethanol | JT Baker | 9000 | |
Forceps | Millipore | 620006 | |
Glass beads | Sigma | Z265926 | |
Glass handle | Sigma | S4647 | |
Glycerol | JT BAKER | 2136-01 | |
Helium tank grade 5 (99.99 %) | - | - | |
HSTaq Kit | PCR BIO | ||
Microcentrifugue | Eppendorf | 022620100 | |
NdeI | New England BioLabs | R0111L | |
Orbital shaker | New Brunswick scientific | NB-G25 | |
PCR tubes | Axygen | PCR-02-C | |
PDS-1000/He TM Biolistic Particle Delivery System | BIO-RAD | 165-2257 | |
Petri dishes (100X10) | BD | 252777 | |
QIAprep Spin Miniprep | Qiagen | 27106 | |
Raffinose | Formedium | RAF03 | |
Replica plater | Scienceware | Z363391 | |
Rupture discs 1350 Psi | BIO-RAD | 1652330 | |
Sorbitol | Sigma | S7547 | |
Spermidine | Sigma | S0266 | |
T4 DNA Ligase | Thermo Scientific | EL0011 | |
Tissue Culture Rotator | Thermo Scientific | 88882015 | |
Tungsten microcarriers M10 | BIO-RAD | 1652266 | |
Vaccum pump of 100L/min capacity | - | - | |
Velvet pads | Bel-Art | H37848-0002 | |
Vortex | Scientifc Industries | SI-0236 | |
Wood aplicator stick | PROMA | 1820060 | |
Yeast extract | BD | 212750 | |
Yeast Nitrogen base without aminoacids | BD | 291920 |
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