Merging theory and mechanism in studies of gynodioecy

Trends in Ecology and Evolution

Volumn 22, Issue 1, 2007, Pages 17-24

  Delph, Lynda F ^a   Touzet, Pascal ^b   Bailey, Maia F ^a,c  

^a INDIANA UNIVERSITY   (United States)

^b CNRS   (France)

^c CENTRE D ECOLOGIE FONCTIONNELLE ET EVOLUTIVE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOPLASM; FEMINIZATION; GYNODIOECY; PLEIOTROPY; POLYMORPHISM; SEX DETERMINATION;

ALLELE; BIOLOGICAL MODEL; CROP; EVOLUTION; GENDER AND SEX; GENE; GENE REPRESSION; GENETIC POLYMORPHISM; GENETICS; MITOCHONDRIAL GENE; PLANT; REVIEW;

ALLELES; CROPS, AGRICULTURAL; EVOLUTION; GENES, MITOCHONDRIAL; GENES, PLANT; MODELS, BIOLOGICAL; PLANTS; POLYMORPHISM, GENETIC; SEX DETERMINATION (GENETICS); SUPPRESSION, GENETIC;

EID: 33845663144     PISSN: 01695347     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tree.2006.09.013     Document Type: Review

References (70)

1. Darwin, C. (1877) The Different Forms of Flowers on Plants of the Same Species, Murray
2. Gigord L., et al. Evidence for effects of restorer genes on male and female reproductive functions of hermaphrodites in the gynodioecious species Thymus vulgaris L. J. Evol. Biol. 12 (1999) 596-604
3. Dudle D., et al. Genetics of sex determination in the gynodioecious species Lobelia siphilitica: evidence from two populations. Heredity 86 (2001) 265-276
4. Bailey M.F. A cost of restoration of male fertility in a gynodioecious species, Lobelia siphilitica. Evolution 56 (2002) 2178-2186
5. Delph L.F., and Mutikainen P. Tests of why maternal gender affects offspring performance in a gynodioecious species. Evolution 57 (2003) 231-239
6. Murayama K., et al. Variation of female frequency and cytoplasmic male-sterility gene frequency among natural gynodioecious populations of wild radish (Raphanus sativus L.). Mol. Ecol. 13 (2004) 2459-2464
7. Frank S.A. The evolutionary dynamics of cytoplasmic male sterility. Am. Nat. 133 (1989) 345-376
8. Hanson M.R. Plant mitochondrial mutations and male sterility. Annu. Rev. Genet. 25 (1991) 461-486
9. Schnable P.S., and Wise R.P. The molecular basis of cytoplasmic male sterility and fertility restoration. Trends Plant Sci. 3 (1998) 175-180
10. Wise R.P., and Pring D.R. Nuclear-mediated mitochondrial gene regulation and male fertility in higher plants: light at the end of the tunnel?. Proc. Natl. Acad. Sci. U. S. A. 99 (2002) 10240-10242
11. Delph L.F., et al. Seed provisioning in gynodioecious Silene acaulis (Caryophyllaceae). Am. J. Bot. 86 (1999) 140-144
12. Delannay X., et al. Mathematical study of the evolution of gynodioecy with cytoplasmic inheritance under the effect of a nuclear restorer gene. Genetics 99 (1981) 169-181
13. Charlesworth D. A further study of the problem of the maintenance of females in gynodioecious species. Heredity 46 (1981) 27-39
14. Gouyon P.H., et al. Nuclear-cytoplasmic male sterility: single-point equilibria versus limit cycles. Am. Nat. 137 (1991) 498-514
15. Bailey M.F., et al. Modeling gynodioecy: novel scenarios for maintaining polymorphism. Am. Nat. 161 (2003) 762-776
16. Chase C.D., and Gabay-Laughnan S. Cytoplasmic male sterility and fertility restoration by nuclear genes. In: Daniel H., and Chase C.D. (Eds). Molecular Biology and Biotechnology of Plant Organelles (2004), Kluwer 593-621
17. Birky Jr. C.W. The inheritance of genes in mitochondria and chloroplasts: laws, mechanisms, and models. Annu. Rev. Genet. 35 (2001) 125-148
18. Lewis D. Male sterility in natural populations of hermaphrodite plants. New Phytol. 40 (1941) 56-63
19. Jacobs M.S., and Wade M.J. A synthetic review of the theory of gynodioecy. Am. Nat. 161 (2003) 837-851
20. Brown G.G. Unique aspects of cytoplasmic male sterility and fertility restoration in Brassica napus. J. Hered. 90 (1999) 351-356
21. Li X.-Q., et al. Restorer genes for different forms of Brassica cytoplasmic male sterility map to a single nuclear locus that modifies transcripts of several mitochondrial genes. Proc. Natl. Acad. Sci. U. S. A. 95 (1998) 10032-10037
22. Geddy R., et al. Cell-specific regulation of a Brassica napus CMS-associated gene by a nuclear restorer with related effects on a floral homeotic gene promoter. Plant J. 41 (2005) 333-345
23. Singh M., et al. Nuclear genes associated with a single Brassica CMS restorer locus influence transcripts of three different mitochondrial gene regions. Genetics 143 (1996) 505-516
24. Laughnan J.R., and Gabay-Laughnan S. Cytoplasmic male sterility in maize. Annu. Rev. Genet. 17 (1983) 27-48
25. Fauron C.M.R., and Casper M. A second type of normal maize mitochondrial genome: an evolutionary link. Genetics 137 (1994) 875-882
26. Dewey R.E., et al. A mitochondrial protein associated with cytoplasmic male sterility in the T cytoplasm of maize. Proc. Natl. Acad. Sci. U. S. A. 84 (1987) 5374-5378
27. Wise R.P., et al. Mutator-induced mutations of the rfl nuclear fertility restorer of T-cytoplasm maize alter the accumulation of T-urf13 mitochondrial transcripts. Genetics 143 (1996) 1383-1394
28. Dill C.L., et al. Rf8 and Rf* mediate unique T-urf13-transcript accumulation, revealing a conserved motif associated with RNA processing and restoration of pollen fertility restoration in T-cytoplasm maize. Genetics 147 (1997) 1367-1379
29. Cui X., et al. The rf2 nuclear restorer gene of male-sterile T-cytoplasm maize. Science 272 (1996) 1334-1336
30. Liu F., et al. Mitochondrial aldehyde dehydrogenase activity is required for male fertility in maize (Zea mays L.). Plant Cell 13 (2001) 1063-1078
31. Liu F., and Schnable P.S. Functional specialization of maize mitochondrial aldehyde dehydrogenases. Plant Physiol. 130 (2002) 1657-1674
32. Gabay-Laughnan S., et al. Molecular-genetic characterization of CMS-S restorer-of-fertility alleles identified in Mexican teosinte. Genetics 166 (2004) 959-970
33. Wen L., and Chase C.D. Pleiotropic effects of a nuclear restorer-of-fertility locus on mitochondrial transcripts in male-fertile and S male-sterile maize. Curr. Genet. 35 (1999) 521-526
34. Chase C.D., and Gabay-Laughnan S. Exploring mitochondrial-nuclear genome interactions with S male-sterile maize. In: Pandali S.G. (Ed). Recent Research Developments in Genetics Vol. 3 (2003), Research Signpost Genetics 31-41
35. Wen L., et al. A nuclear restorer-of-fertility mutation disrupts accumulation of mitochondrial ATP synthase subunit α in developing pollen of S male-sterile maize. Genetics 165 (2003) 771-779
36. Mackenzie S.A., and Chase C. Fertility restoration in cytoplasmic male sterile Phaseolus vulgaris L. Theor. Appl. Genet. 74 (1990) 642-645
37. Chase C.D., and Ortega V.M. Organization of ATPA coding and 3′ flanking sequences associated with cytoplasmic male sterility in Phaseolus vulgaris L. Curr. Genet. 22 (1992) 147-153
38. Johns C., et al. A mitochondrial DNA sequence is associated with abnormal pollen development in cytoplasmic male sterile bean plants. Plant Cell 4 (1992) 435-449
39. Abad A.R., et al. Specific expression in reproductive tissues and fate of a mitochondrial sterility-associated protein in cytoplasmic male-sterile bean. Plant Cell 7 (1995) 271-285
40. Sarria R., et al. A cytoplasmic male sterility-associated mitochondrial peptide in common bean is post-transcriptionally regulated. Plant Cell 10 (1998) 1217-1228
41. Arrieta-Montiel M., et al. Tracing evolutionary and developmental implications of mitochondrial stoichiometric shifting in the common bean. Genetics 158 (2001) 851-864
42. Mackenzie S.A., and Bassett M.J. Genetics of fertility restoration in cytoplasmic male sterile Phaseolus vulgaris L. 1. Cytoplasmic alteration by a nuclear restorer gene. Theor. Appl. Genet. 74 (1987) 642-645
43. Janska H., et al. Stoichiometric shifts in the common bean mitochondrial genome leading to male sterility and spontaneous reversion to fertility. Plant Cell 10 (1998) 1163-1180
44. Mackenzie S.A. Identification of a sterility-inducing cytoplasm in a fertile accession line of Phaseolus vulgaris L. Genetics 127 (1991) 411-416
45. Chase C.D. Expression of CMS-unique and flanking mitochondrial DNA sequences in Phaseolus vulgaris L. Curr. Genet. 25 (1994) 245-251
46. Jia M.H., et al. Nuclear fertility restorer genes map to the same linkage group in cytoplasmic male-sterile bean. Theor. Appl. Genet. 95 (1997) 205-210
47. Wang Z., et al. Cytoplasmic male sterility of rice with Boro II cytoplasm is caused by a cytotoxic peptide and is restored by two related PPR motif genes via distinct modes of mRNA silencing. Plant Cell 18 (2006) 676-687
48. Wiesenberger G., and Fox T.D. Pet127p, a membrane-associated protein involved in stability and processing of Saccharomyces cerevisiae mitochondrial RNAs. Mol. Cell Biol. 17 (1997) 2816-2824
49. Touzet P., and Budar F. Unveiling the molecular arms race between two conflicting genomes in cytoplasmic male sterility?. Trends Plant Sci. 9 (2004) 568-570
50. Ross M.D., and Gregorius H.R. Selection with gene-cytoplasm interactions. II. Maintenance of gynodioecy. Genetics 109 (1985) 427-439
51. Bellaoui M., et al. The steady-state level of mRNA from the Ogura cytoplasmic male sterility locus in Brassica cybrids is determined post-transcriptionally by its 3′ region. EMBO J. 16 (1997) 5057-5068
52. Hanson M.R., and Bentolila S. Interactions of mitochondrial and nuclear genes that affect male gametophyte development. Plant Cell 16 (2004) S154-S169
53. Leclercq P. Identification de gènes de restauration de fertilité sur cytoplasmes stérilisants chez le tournesol. Agronomie 4 (1984) 573-576
54. Monéger F., et al. Nuclear restoration of cytoplasmic male sterility in sunflower is associated with the tissue-specific regulation of a novel mitochondrial gene. EMBO J. 13 (1994) 8-17
55. Gagliardi D., and Leaver C.J. Polyadenylation accelerates the degradation of the mitochondrial mRNA associated with cytoplasmic male sterility in sunflower. EMBO J. 18 (1999) 3757-3766
56. 0-ATP synthase: insight into the basis of cytoplasmic male sterility in sunflower. EMBO Rep. 4 (2003) 381-386
57. Young E.G., and Hanson M.R. A fused mitochondrial gene associated with cytoplasmic male sterility is developmentally regulated. Cell 50 (1987) 41-49
58. Nivison H.T., and Hanson M.R. Identification of a mitochondrial protein associated with cytoplasmic male sterility in Petunia. Plant Cell 1 (1989) 1121-1130
59. Pruitt K.D., and Hanson M.R. Transcription of the petunia mitochondrial CMS-associated Pcf locus in male sterile and fertility-restored lines. Mol. Gen. Genet. 227 (1991) 348-355
60. Hanson M.R., et al. Mitochondrial gene organization and expression in petunia male fertile and sterile plants. J. Hered. 90 (1999) 362-368
61. Bentolila S., et al. A pentatricopeptide repeat-containing gene restores fertility to cytoplasmic male-sterile plants. Proc. Natl. Acad. Sci. U. S. A. 99 (2002) 10887-10892
62. Bellaoui M., et al. The restorer Rfo gene acts post-transcriptionally on the stability of the ORF138 Ogura CMS-associated protein in reproductive tissues of rapeseed cybrids. Plant Mol. Biol. 40 (1999) 893-902
63. Budar F., and Pelletier G. Male sterility in plants: occurrence, determinism, significance and use. C. R. Acad. Sci. III 324 (2001) 5443-5550
64. Iwabuchi M., et al. Processing followed by complete editing of an altered atp6 RNA restores fertility of cytoplasmic male sterile rice. EMBO J. 12 (1993) 1437-1446
65. Akagi H., et al. A unique sequence located downstream from the rice mitochondrial atp6 may cause male sterility. Curr. Genet. 25 (1994) 52-58
66. Komori T., et al. Map-based cloning of a fertility restorer gene, Rf-1, in rice (Oryza sativa L.). Plant J. 37 (2004) 315-325
67. Tang H.V., et al. Transcript processing internal to a mitochondrial open reading frame is correlated with fertility restoration in male-sterile sorghum. Plant J. 10 (1996) 123-133
68. Tang H.V., et al. Cosegregation of single genes associated with fertility restoration and transcript processing of sorghum mitochondrial orf107 and urf209. Genetics 150 (1998) 383-391
69. Pring D.R., et al. A unique two-gene gametophytic male sterility system in sorghum involving a possible role of RNA editing in fertility restoration. J. Hered. 90 (1999) 386-393
70. Pring D.R., and Tang H.V. Transcript profiling of male-fertile and male-sterile sorghum indicated extensive alterations in gene expression during microgametogenesis. Sex. Plant Reprod. 16 (2004) 289-297