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Mating types are the microorganism equivalent to sexes in multicellular lifeforms and are thought to be the ancestor to distinct sexes. They also occur in multicellular organisms such as fungi.
Definition
Mating types are the microorganism equivalent to sex in higher organisms and occur in isogamous species. Depending on the group, different mating types are often referred to by numbers, letters, or simply "+" and "−" instead of "male" and "female", which refer to "sexes" or differences in size between gametes.Syngamy can only take place between gametes carrying different mating types.
Mating types are extensively studied in fungi. Among fungi, mating type is determined by chromosomal regions called mating-type loci. Furthermore, it is not as simple as "two different mating types can mate", but rather, a matter of combinatorics. As a simple example, most basidiomycete have a "tetrapolar heterothallism" mating system: there are two loci, and mating between two individuals is possible if the alleles on both loci are different. For example, if there are 3 alleles per locus, then there would be 9 mating types, each of which can mate with 4 other mating types. By multiplicative combination, it generates a vast number of mating types.
Mechanism
As an illustration, the model organism Coprinus cinereus has two mating-type loci called A and B. Both loci have 3 groups of genes. At the A locus are 6 homeodomain proteins arranged in 3 groups of 2 (HD1 and HD2), which arose by gene duplication. At the B locus, each of the 3 groups contain one pheromone G-protein-coupled receptor and usually two genes for pheromones.
The A locus ensures heterothallism through a specific interaction between HD1 and HD2 proteins. Within each group, a HD1 protein can only form a functional heterodimer with a HD2 protein from a different group, not with the HD2 protein from its own group. Functional heterodimers are necessary for a dikaryon-specific transcription factor, and its lack arrests the development process. They function redundantly, so it is only necessary for one of the three groups to be heterozygotic for the A locus to work.
Similarly, the B locus ensures heterothallism through a specific interaction between pheromone receptors and pheromones. Each pheromone receptor is activated by pheromones from other groups, but not by the pheromone encoded by the same group. This means that a pheromone receptor can only trigger a signaling cascade when it binds to a pheromone from a different group, not when it binds to the pheromone from its own group. They also function redundantly.
In both cases, the mechanism is based on a "self-incompatibility" principle, where the proteins or pheromones from the same group are incompatible with each other, but compatible with those from different groups.
Similarly, the Schizophyllum commune has 2 gene groups (Aα, Aβ) for homeodomain proteins on the A locus, and 2 gene groups (Bα, Bβ) for pheromones and receptors on the B locus. Aα has 9 alleles, Aβ has 32, Bα has 9, and Bβ has 9. The two gene groups at the A locus function independently but redundantly, so only one group out of the two needs to be heterozygotic for it to work. Similarly for the two gene groups at the B locus. Thus, mating between two individuals succeeds if
Thus there are mating types, each of which can mate with
other mating types.
Occurrence
Reproduction by mating types is especially prevalent in fungi. Filamentous ascomycetes usually have two mating types referred to as "MAT1-1" and "MAT1-2", following the yeast mating-type locus (MAT). Under standard nomenclature, MAT1-1 (which may informally be called MAT1) encodes for a regulatory protein with an alpha box motif, while MAT1-2 (informally called MAT2) encodes for a protein with a high motility-group (HMG) DNA-binding motif, as in the yeast mating type MATα1. The corresponding mating types in yeast, a non-filamentous ascomycete, are referred to as MATa and MATα.
Mating type genes in ascomycetes are called idiomorphs rather than alleles due to the uncertainty of the origin by common descent. The proteins they encode are transcription factors which regulate both the early and late stages of the sexual cycle. Heterothallic ascomycetes produce gametes, which present a single Mat idiomorph, and syngamy will only be possible between gametes carrying complementary mating types. On the other hand, homothallic ascomycetes produce gametes that can fuse with every other gamete in the population (including its own mitotic descendants) most often because each haploid contains the two alternate forms of the Mat locus in its genome.
Basidiomycetes can have thousands of different mating types.
In the ascomycete Neurospora crassa matings are restricted to interaction of strains of opposite mating type. This promotes some degree of outcrossing. Outcrossing, through complementation, could provide the benefit of masking recessive deleterious mutations in genes which function in the dikaryon and/or diploid stage of the life cycle.
Evolution
Mating types likely predate anisogamy, and sexes evolved directly from mating types or independently in some lineages.
Studies on green algae have provided evidence for the evolutionary link between sexes and mating types. In 2006 Japanese researchers found a gene in males of Pleodorina starrii that is an orthologue to a gene for a mating type in the Chlamydomonas reinhardtii. In Volvocales, the plus mating type is the ancestor to female.
In ciliates, multiple mating types evolved from binary mating types in several lineages.: 75 As of 2019, genomic conflict has been considered the leading explanation for the evolution of two mating types.
Secondary mating types evolved alongside simultaneous hermaphrodites in several lineages.: 71 [clarification needed]
See also
- Mating in fungi
- Mating of yeast
- Mating-type locus
- Saccharomyces cerevisiae (a and α mating types)
- Schizophyllum commune (23,328 mating types)
- Tetrahymena (7 mating types)
References
- "mating type". Oxford Reference. Retrieved 2021-08-26.
- From Mating Types to Sexes. Bachtrog D, Mank JE, Peichel CL, Kirkpatrick M, Otto SP, et al. (2014) Sex Determination: Why So Many Ways of Doing It? PLoS Biol 12(7): e1001899. doi:10.1371/journal.pbio.1001899
- Idnurm, Alexander; Hood, Michael E.; Johannesson, Hanna; Giraud, Tatiana (2015-12-01). "Contrasted patterns in mating-type chromosomes in fungi: Hotspots versus coldspots of recombination". Fungal Biology Reviews. Special Issue: Fungal sex and mushrooms – A credit to Lorna Casselton. 29 (3): 220–229. doi:10.1016/j.fbr.2015.06.001. ISSN 1749-4613. PMC 4680991.
- Kamada, Takashi (May 2002). "Molecular genetics of sexual development in the mushroom Coprinus cinereus". BioEssays. 24 (5): 449–459. doi:10.1002/bies.10083. ISSN 0265-9247.
- Riquelme, Meritxell; Challen, Michael P; Casselton, Lorna A; Brown, Andrew J (2005-07-01). "The Origin of Multiple B Mating Specificities in Coprinus cinereus". Genetics. 170 (3): 1105–1119. doi:10.1534/genetics.105.040774. ISSN 1943-2631. PMC 1451185. PMID 15879506.
- Brown, Andrew J.; Casselton, Lorna A. (2001-07-01). "Mating in mushrooms: increasing the chances but prolonging the affair". Trends in Genetics. 17 (7): 393–400. doi:10.1016/S0168-9525(01)02343-5. ISSN 0168-9525.
- Kothe, Erika (1996). "Tetrapolar fungal mating types: Sexes by the thousands". FEMS Microbiology Reviews. 18 (1): 65–87. doi:10.1016/0168-6445(96)00003-4. PMID 8672296.
- Yoder, O.C.; Valent, Barbara; Chumley, Forrest (1986). "Genetic Nomenclature and Practice for Plant Pathogenic Fungi" (PDF). Phytopathology. 76 (4): 383–385. doi:10.1094/phyto-76-383. Retrieved 11 November 2015.
- Turgeon, B.G.; Yoder, O.C. (2000). "Proposed Nomenclature for Mating Type Genes of Filamentous Ascomycetes". Fungal Genetics and Biology. 31 (1): 1–5. doi:10.1006/fgbi.2000.1227. PMID 11118130.
- Hanson, Sara J; Wolfe, Kenneth H (2017-05-01). "An Evolutionary Perspective on Yeast Mating-Type Switching". Genetics. 206 (1): 9–32. doi:10.1534/genetics.117.202036. ISSN 1943-2631. PMC 5419495. PMID 28476860.
- Giraud, T.; et al. (2008). "Mating system of the anther smut fungus Microbotryum violaceum: Selfing under heterothallism". Eukaryotic Cell. 7 (5): 765–775. doi:10.1128/ec.00440-07. PMC 2394975. PMID 18281603.
- Casselton LA (2002). "Mate recognition in fungi". Heredity. 88 (2): 142–147. doi:10.1038/sj.hdy.6800035. PMID 11932772.
- Bernstein H, Byerly HC, Hopf FA, Michod RE. Genetic damage, mutation, and the evolution of sex. Science. 1985 Sep 20;229(4719):1277-81. doi: 10.1126/science.3898363. PMID 3898363
- Andersson, Malte (1994-06-16). Sexual Selection. Princeton University Press. p. 4. ISBN 978-0-691-00057-2.
- Perrin, Nicolas (2012-04-06). "What Uses Are Mating Types? The "Developmental Switch" Model". Evolution. 66 (4): 947–956. doi:10.1111/j.1558-5646.2011.01562.x. PMID 22486681. S2CID 5798638.
- Sawada, Hitoshi; Inoue, Naokazu; Iwano, Megumi (2014). Sexual Reproduction in Animals and Plants. Springer. pp. 215–227. ISBN 978-4-431-54589-7.
- Nozaki, Hisayoshi; Mori, Toshiyuki; Misumi, Osami; Matsunaga, Sachihiro; Kuroiwa, Tsuneyoshi (2006-12-19). "Males evolved from the dominant isogametic mating type". Current Biology. 16 (24): R1018–1020. Bibcode:2006CBio...16R1018N. doi:10.1016/j.cub.2006.11.019. ISSN 0960-9822. PMID 17174904. S2CID 15748275.
- Togashi, Tatsuya; Cox, Paul Alan (2011-04-14). The Evolution of Anisogamy: A Fundamental Phenomenon Underlying Sexual Selection. Cambridge University Press. pp. 1–15. ISBN 978-1-139-50082-1.
- Beukeboom, Leo W.; Perrin, Nicolas (2014). The Evolution of Sex Determination. Oxford University Press. ISBN 978-0-19-965714-8.
- Hill, Geoffrey E. (2019-04-30). Mitonuclear Ecology. Oxford University Press. p. 115. ISBN 978-0-19-881825-0.
Mating types are the microorganism equivalent to sexes in multicellular lifeforms and are thought to be the ancestor to distinct sexes They also occur in multicellular organisms such as fungi DefinitionMating types are the microorganism equivalent to sex in higher organisms and occur in isogamous species Depending on the group different mating types are often referred to by numbers letters or simply and instead of male and female which refer to sexes or differences in size between gametes Syngamy can only take place between gametes carrying different mating types Mating types are extensively studied in fungi Among fungi mating type is determined by chromosomal regions called mating type loci Furthermore it is not as simple as two different mating types can mate but rather a matter of combinatorics As a simple example most basidiomycete have a tetrapolar heterothallism mating system there are two loci and mating between two individuals is possible if the alleles on both loci are different For example if there are 3 alleles per locus then there would be 9 mating types each of which can mate with 4 other mating types By multiplicative combination it generates a vast number of mating types MechanismAs an illustration the model organism Coprinus cinereus has two mating type loci called A and B Both loci have 3 groups of genes At the A locus are 6 homeodomain proteins arranged in 3 groups of 2 HD1 and HD2 which arose by gene duplication At the B locus each of the 3 groups contain one pheromone G protein coupled receptor and usually two genes for pheromones The A locus ensures heterothallism through a specific interaction between HD1 and HD2 proteins Within each group a HD1 protein can only form a functional heterodimer with a HD2 protein from a different group not with the HD2 protein from its own group Functional heterodimers are necessary for a dikaryon specific transcription factor and its lack arrests the development process They function redundantly so it is only necessary for one of the three groups to be heterozygotic for the A locus to work Similarly the B locus ensures heterothallism through a specific interaction between pheromone receptors and pheromones Each pheromone receptor is activated by pheromones from other groups but not by the pheromone encoded by the same group This means that a pheromone receptor can only trigger a signaling cascade when it binds to a pheromone from a different group not when it binds to the pheromone from its own group They also function redundantly In both cases the mechanism is based on a self incompatibility principle where the proteins or pheromones from the same group are incompatible with each other but compatible with those from different groups Similarly the Schizophyllum commune has 2 gene groups Aa Ab for homeodomain proteins on the A locus and 2 gene groups Ba Bb for pheromones and receptors on the B locus Aa has 9 alleles Ab has 32 Ba has 9 and Bb has 9 The two gene groups at the A locus function independently but redundantly so only one group out of the two needs to be heterozygotic for it to work Similarly for the two gene groups at the B locus Thus mating between two individuals succeeds if Aa1 Aa2 OR Ab1 Ab2 AND Ba1 Ba2 OR Bb1 Bb2 displaystyle A alpha 1 neq A alpha 2 mathrm OR A beta 1 neq A beta 2 mathrm AND B alpha 1 neq B alpha 2 mathrm OR B beta 1 neq B beta 2 Thus there are 9 32 9 9 23328 displaystyle 9 times 32 times 9 times 9 23328 mating types each of which can mate with 9 32 1 9 9 1 22960 displaystyle 9 times 32 1 times 9 times 9 1 22960 other mating types OccurrenceReproduction by mating types is especially prevalent in fungi Filamentous ascomycetes usually have two mating types referred to as MAT1 1 and MAT1 2 following the yeast mating type locus MAT Under standard nomenclature MAT1 1 which may informally be called MAT1 encodes for a regulatory protein with an alpha box motif while MAT1 2 informally called MAT2 encodes for a protein with a high motility group HMG DNA binding motif as in the yeast mating type MATa1 The corresponding mating types in yeast a non filamentous ascomycete are referred to as MATa and MATa Mating type genes in ascomycetes are called idiomorphs rather than alleles due to the uncertainty of the origin by common descent The proteins they encode are transcription factors which regulate both the early and late stages of the sexual cycle Heterothallic ascomycetes produce gametes which present a single Mat idiomorph and syngamy will only be possible between gametes carrying complementary mating types On the other hand homothallic ascomycetes produce gametes that can fuse with every other gamete in the population including its own mitotic descendants most often because each haploid contains the two alternate forms of the Mat locus in its genome Basidiomycetes can have thousands of different mating types In the ascomycete Neurospora crassa matings are restricted to interaction of strains of opposite mating type This promotes some degree of outcrossing Outcrossing through complementation could provide the benefit of masking recessive deleterious mutations in genes which function in the dikaryon and or diploid stage of the life cycle EvolutionMating types likely predate anisogamy and sexes evolved directly from mating types or independently in some lineages Studies on green algae have provided evidence for the evolutionary link between sexes and mating types In 2006 Japanese researchers found a gene in males of Pleodorina starrii that is an orthologue to a gene for a mating type in the Chlamydomonas reinhardtii In Volvocales the plus mating type is the ancestor to female In ciliates multiple mating types evolved from binary mating types in several lineages 75 As of 2019 genomic conflict has been considered the leading explanation for the evolution of two mating types Secondary mating types evolved alongside simultaneous hermaphrodites in several lineages 71 clarification needed See alsoMating in fungi Mating of yeast Mating type locus Saccharomyces cerevisiae a and a mating types Schizophyllum commune 23 328 mating types Tetrahymena 7 mating types References mating type Oxford Reference Retrieved 2021 08 26 From Mating Types to Sexes Bachtrog D Mank JE Peichel CL Kirkpatrick M Otto SP et al 2014 Sex Determination Why So Many Ways of Doing It PLoS Biol 12 7 e1001899 doi 10 1371 journal pbio 1001899 Idnurm Alexander Hood Michael E Johannesson Hanna Giraud Tatiana 2015 12 01 Contrasted patterns in mating type chromosomes in fungi Hotspots versus coldspots of recombination Fungal Biology Reviews Special Issue Fungal sex and mushrooms A credit to Lorna Casselton 29 3 220 229 doi 10 1016 j fbr 2015 06 001 ISSN 1749 4613 PMC 4680991 Kamada Takashi May 2002 Molecular genetics of sexual development in the mushroom Coprinus cinereus BioEssays 24 5 449 459 doi 10 1002 bies 10083 ISSN 0265 9247 Riquelme Meritxell Challen Michael P Casselton Lorna A Brown Andrew J 2005 07 01 The Origin of Multiple B Mating Specificities in Coprinus cinereus Genetics 170 3 1105 1119 doi 10 1534 genetics 105 040774 ISSN 1943 2631 PMC 1451185 PMID 15879506 Brown Andrew J Casselton Lorna A 2001 07 01 Mating in mushrooms increasing the chances but prolonging the affair Trends in Genetics 17 7 393 400 doi 10 1016 S0168 9525 01 02343 5 ISSN 0168 9525 Kothe Erika 1996 Tetrapolar fungal mating types Sexes by the thousands FEMS Microbiology Reviews 18 1 65 87 doi 10 1016 0168 6445 96 00003 4 PMID 8672296 Yoder O C Valent Barbara Chumley Forrest 1986 Genetic Nomenclature and Practice for Plant Pathogenic Fungi PDF Phytopathology 76 4 383 385 doi 10 1094 phyto 76 383 Retrieved 11 November 2015 Turgeon B G Yoder O C 2000 Proposed Nomenclature for Mating Type Genes of Filamentous Ascomycetes Fungal Genetics and Biology 31 1 1 5 doi 10 1006 fgbi 2000 1227 PMID 11118130 Hanson Sara J Wolfe Kenneth H 2017 05 01 An Evolutionary Perspective on Yeast Mating Type Switching Genetics 206 1 9 32 doi 10 1534 genetics 117 202036 ISSN 1943 2631 PMC 5419495 PMID 28476860 Giraud T et al 2008 Mating system of the anther smut fungus Microbotryum violaceum Selfing under heterothallism Eukaryotic Cell 7 5 765 775 doi 10 1128 ec 00440 07 PMC 2394975 PMID 18281603 Casselton LA 2002 Mate recognition in fungi Heredity 88 2 142 147 doi 10 1038 sj hdy 6800035 PMID 11932772 Bernstein H Byerly HC Hopf FA Michod RE Genetic damage mutation and the evolution of sex Science 1985 Sep 20 229 4719 1277 81 doi 10 1126 science 3898363 PMID 3898363 Andersson Malte 1994 06 16 Sexual Selection Princeton University Press p 4 ISBN 978 0 691 00057 2 Perrin Nicolas 2012 04 06 What Uses Are Mating Types The Developmental Switch Model Evolution 66 4 947 956 doi 10 1111 j 1558 5646 2011 01562 x PMID 22486681 S2CID 5798638 Sawada Hitoshi Inoue Naokazu Iwano Megumi 2014 Sexual Reproduction in Animals and Plants Springer pp 215 227 ISBN 978 4 431 54589 7 Nozaki Hisayoshi Mori Toshiyuki Misumi Osami Matsunaga Sachihiro Kuroiwa Tsuneyoshi 2006 12 19 Males evolved from the dominant isogametic mating type Current Biology 16 24 R1018 1020 Bibcode 2006CBio 16R1018N doi 10 1016 j cub 2006 11 019 ISSN 0960 9822 PMID 17174904 S2CID 15748275 Togashi Tatsuya Cox Paul Alan 2011 04 14 The Evolution of Anisogamy A Fundamental Phenomenon Underlying Sexual Selection Cambridge University Press pp 1 15 ISBN 978 1 139 50082 1 Beukeboom Leo W Perrin Nicolas 2014 The Evolution of Sex Determination Oxford University Press ISBN 978 0 19 965714 8 Hill Geoffrey E 2019 04 30 Mitonuclear Ecology Oxford University Press p 115 ISBN 978 0 19 881825 0