Molecular Communication: An acid tale of prion formation
The transformation of grape juice into an appetising alcoholic beverage is not as straightforward as one might imagine. The yeast Saccharomyces cerevisiae is responsible for fermenting the sugars naturally found in grapes to make ethanol and carbon dioxide. Yet grapes, like many fruits, also contain L-malic acid, which has a sour taste, so the winemaker must trigger a process known as malolactic fermentation to turn the offending L-malic acid into the more palatable and ‘softer’ tasting L-lactic acid.
A variety of bacteria carry out the malolactic fermentation. Such bacteria may already be present on the skin of the grapes or the winemaker can add them after the alcoholic fermentation has taken place. Oenococcus oeni is the bacterium of choice for winemakers, partly because – unlike many other bacteria that produce lactic acid – it does not inhibit the ability of the yeast to ferment sugars.
Louis Pasteur first noted that lactic acid-producing bacteria are often associated with failed wine fermentations over 140 years ago (Pasteur, 1873; Alexandre et al., 2004). Yet, we are only now beginning to understand the complexity of the interplay between these bacteria and yeast during winemaking, thanks largely to the work of the late Susan Lindquist (who died only last month), and Daniel Jarosz, who is now at Stanford University School of Medicine. Now, in eLife, David Garcia of Stanford, David Dietrich and Jon Clardy of Harvard Medical School, and Jarosz report that lactic acid produced by certain bacteria can trigger the formation of the [GAR+] prion in fermenting yeast (Garcia et al., 2016).
Prions are made when proteins undergo a change in conformation and activity that they can sustain themselves and help other proteins to adopt. This in turn gives rise to a heritable form of the protein (known as the amyloid form) that assembles into clumps. However, unlike other yeast prions, the transmission of [GAR+] from cell to cell is not associated with a heritable amyloid. Rather, two other proteins contribute to the formation of the [GAR+] prion in yeast cells (Brown and Lindquist, 2009). But what has the [GAR+] prion got to do with lactic acid and failed wine fermentations?
The [GAR+] prion triggers a remarkable reprogramming of the carbohydrate metabolism in the host cell. By overriding an ancient mechanism that promotes the breakdown of glucose over other sources of carbon, [GAR+] cells are able to metabolise a wide range of other carbon sources, even when glucose is present (Brown and Lindquist, 2009). This is bad news for the winemaker because [GAR+] cells generate less ethanol, which aids the growth of lactic acid-producing bacteria (Figure 1).
Earlier studies by Jarosz and Lindquist found that a wide range of bacteria secrete a chemical messenger (with a low molecular weight) that induces the appearance of [GAR+] in several different yeast species (Jarosz et al., 2014a, 2014b). Since this messenger was resistant to digestion by enzymes, researchers assumed that it was a metabolite. Garcia et al. now report that L-lactic acid can serve as this messenger.
This is not to say that L-lactic acid is the only messenger. Moreover, it is striking that a number of lactic acid-producing bacteria do not induce the [GAR+] prion. These include O. oeni (Jarosz et al., 2014b), whose inability to induce the prion may well contribute to its suitability for wine production. It has been known for over 50 years that the interactions between yeast and the bacteria involved in malolactic fermentation depend on the combinations of species present (Fornachon, 1968), and now we better understand why such variation exists.
The physical structure of the [GAR+] prion and the method by which lactic acid induces its formation remain to be established. However, the new communication mechanism discovered by Garcia et al. is important because it is beneficial to both yeast and bacteria in their native environments, and because it finally explains an observation first made by Pasteur over 140 years ago.
References
-
Saccharomyces cerevisiae-Oenococcus oeni interactions in wine: current knowledge and perspectivesInternational Journal of Food Microbiology 93:141–154.https://doi.org/10.1016/j.ijfoodmicro.2003.10.013
-
A heritable switch in carbon source utilization driven by an unusual yeast prionGenes & Development 23:2320–2332.https://doi.org/10.1101/gad.1839109
-
Influence of different yeasts on the growth of lactic acid bacteria in wineJournal of the Science of Food and Agriculture 19:374–378.https://doi.org/10.1002/jsfa.2740190705
-
BookEtudes Sure Le Vin, Ses Maladies, Causes Qui Les Provoquent Procedes Nouveau Pour Le Conserver Et Pour Le Vieillir (2nd Edition)Paris: Librairie F. Savy.
Article and author information
Author details
Publication history
Copyright
© 2016, Tuite
This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.
Metrics
-
- 2,611
- views
-
- 180
- downloads
-
- 2
- citations
Views, downloads and citations are aggregated across all versions of this paper published by eLife.
Download links
Downloads (link to download the article as PDF)
Open citations (links to open the citations from this article in various online reference manager services)
Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)
Further reading
-
- Chromosomes and Gene Expression
Cells evoke the DNA damage checkpoint (DDC) to inhibit mitosis in the presence of DNA double-strand breaks (DSBs) to allow more time for DNA repair. In budding yeast, a single irreparable DSB is sufficient to activate the DDC and induce cell cycle arrest prior to anaphase for about 12–15 hr, after which cells ‘adapt’ to the damage by extinguishing the DDC and resuming the cell cycle. While activation of the DNA damage-dependent cell cycle arrest is well understood, how it is maintained remains unclear. To address this, we conditionally depleted key DDC proteins after the DDC was fully activated and monitored changes in the maintenance of cell cycle arrest. Degradation of Ddc2ATRIP, Rad9, Rad24, or Rad53CHK2 results in premature resumption of the cell cycle, indicating that these DDC factors are required both to establish and maintain the arrest. Dun1 is required for the establishment, but not the maintenance, of arrest, whereas Chk1 is required for prolonged maintenance but not for initial establishment of the mitotic arrest. When the cells are challenged with two persistent DSBs, they remain permanently arrested. This permanent arrest is initially dependent on the continuous presence of Ddc2, Rad9, and Rad53; however, after 15 hr these proteins become dispensable. Instead, the continued mitotic arrest is sustained by spindle assembly checkpoint (SAC) proteins Mad1, Mad2, and Bub2 but not by Bub2’s binding partner Bfa1. These data suggest that prolonged cell cycle arrest in response to 2 DSBs is achieved by a handoff from the DDC to specific components of the SAC. Furthermore, the establishment and maintenance of DNA damage-induced cell cycle arrest require overlapping but different sets of factors.
-
- Chromosomes and Gene Expression
- Developmental Biology
About 70% of human cleavage stage embryos show chromosomal mosaicism, falling to 20% in blastocysts. Chromosomally mosaic human blastocysts can implant and lead to healthy new-borns with normal karyotypes. Studies in mouse embryos and human gastruloids showed that aneuploid cells are eliminated from the epiblast by p53-mediated apoptosis while being tolerated in the trophectoderm. These observations suggest a selective loss of aneuploid cells from human embryos, but the underlying mechanisms are not yet fully understood. Here, we investigated the cellular consequences of aneuploidy in a total of 125 human blastocysts. RNA-sequencing of trophectoderm cells showed activated p53 pathway and apoptosis proportionate to the level of chromosomal imbalance. Immunostaining corroborated that aneuploidy triggers proteotoxic stress, autophagy, p53-signaling, and apoptosis independent from DNA damage. Total cell numbers were lower in aneuploid embryos, due to a decline both in trophectoderm and in epiblast/primitive endoderm cell numbers. While lower cell numbers in trophectoderm may be attributed to apoptosis, aneuploidy impaired the second lineage segregation, particularly primitive endoderm formation. This might be reinforced by retention of NANOG. Our findings might explain why fully aneuploid embryos fail to further develop and we hypothesize that the same mechanisms lead to the removal of aneuploid cells from mosaic embryos.