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Pollen–pistil barriers to crossing in maize and teosinte result from incongruity rather than active rejection

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Abstract

Many popcorn strains cannot be fertilized by pollen of dent and flint strains although the reciprocal crosses are successful. Similarly, plants of some annual teosinte populations can fertilize maize but do not accept its pollen. Single genes or gene complexes govern these two unilateral barriers to crossing. Failure of fertilization could reflect active rejection by the pistil of pollen containing a contrasting allele (incompatibility). Alternatively, the pistil could require presence of a matching allele in pollen (congruity). To distinguish between these possibilities genetically, the receptivity to pollen having both alleles was determined. If there is active rejection, heteroallelic pollen would not be accepted; if presence of a matching allele is required, heteroallelic pollen would be accepted. In both the popcorn and teosinte crossing barrier systems, heteroallelic pollen functioned, consistent with the congruity model.

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References

  • Asher PD, Peloquin SJ (1968) Pollen tube growth and incompatibility following intra- and inter-specific pollinations in Lilium longiflorum. Am J Bot 55:1230–1234

    Article  Google Scholar 

  • Auger DL, Birchler JA (2002) Maize tertiary trisomic stocks derived from B-A translocations. J Heredity 93:42–47

    Article  CAS  Google Scholar 

  • Beckett JB (1983) Kernel-weight effects and transmission of a partial trisome involving the long arm of chromosome 5 in maize. Can J Genet Cytol 25:346–353

    Google Scholar 

  • Beckett JB (1991) Cytogenetic, genetic and plant breeding applications of B-A translocations in maize. In: Gupta PK, Tsuchiya T (eds) Chromosome engineering in plants: genetics, breeding, evolution, vol 2A. Elsevier, Amsterdam, pp 493–529

  • Bernacchi D, Tanksley SD (1997) An interspecific backcross of Lycopersion esculentum × L. hirsutum: linkage analysis and a QTL study of sexual compatibility factors and floral traits. Genetics 147:861–877

    PubMed  CAS  Google Scholar 

  • Birchler JA (1993) Trisomic manipulation. In: Freeling M, Walbot V (eds) The maize handbook. Springer, Berlin Heidelberg New York, pp 302–308

    Google Scholar 

  • de Nettancourt D (2001) Incompatibility and incongruity in wild and cultivated plants. 2nd edn. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Edlund AF, Swanson R, Preuss D (2004) Pollen and stigma structure and function: the role of diversity in pollination. Plant Cell 16:S84–S97

    Article  PubMed  CAS  Google Scholar 

  • Emerson RA (1934) Relation of the differential fertilization genes, Ga ga, to certain other genes of the Su-Tu lineage group of maize. Genetics 19:137–156

    PubMed  CAS  Google Scholar 

  • Evans MMS, Kermicle JL (2001) Teosinte crossing barrier 1, a locus governing hybridization of teosinte with maize. Theor Appl Genet 103:259–265

    Article  CAS  Google Scholar 

  • Franklin-Tong VE, Franklin FCH (2003) The different mechanisms of gametophytic self-incompatibility. Phil Trans R Soc Lond Ser B 358:1025–1032

    Article  CAS  Google Scholar 

  • Grun P, Aubertin M (1966) The inheritance and expression of unilateral incompatibility in Solanum. Heredity 21:131–138

    Google Scholar 

  • Hancock CN, Kondo K, Beecher B, McClure B (2003) The S-locus and unilateral incompatibility. Phil Trans R Soc Lond Ser B 358:1133–1140

    Article  CAS  Google Scholar 

  • Hermsen JGTh, Olsder J, Jansen P, Hoving E (1974) Acceptance of self-compatible pollen from Solanum verrocosum in dihaploids from S. tuberosum. In: Linskens HF (ed) Fertilization in higher plants. North Holland, Amsterdam, pp 37–40

    Google Scholar 

  • Hogenboom NG (1972) Breaking breeding barriers in Lycopersicon. 5. The inheritance of the unilateral incompatibility between L. peruvianum (L.) Mill. and L. esculentum Mill. and the genetics of its breakdown. Euphytica 21:405–414

    Article  Google Scholar 

  • Hogenboom NG (1975) Incompatibility and incongruity: two different mechanisms for the non-functioning of intimate partner relationships. Proc R Soc Lon B 188:361–375

    Google Scholar 

  • Hogenboom NG (1984) Incongruity: non-functioning of intercellular and intracellular partner relationships through non-matching information. In: Linskens HF, Heslop-Harrison J (eds) Encyclopedia of plant physiology. Springer, Berlin Heidelberg New York, pp 640–654

    Google Scholar 

  • Jones DF (1920) Selective fertilization in pollen mixtures. Biol Bulletin 38:251–289

    Article  Google Scholar 

  • Kao T-h, Tsukamoto T (2004) The molecular and genetic basis of S-RNase-based self-incompatibility. Plant Cell 16:S72–S83

    Article  PubMed  Google Scholar 

  • Kachroo A, Nasrallah ME, Nasrallah JB (2002) Self-incompatibility in the Brassicaceae: receptor-ligand signaling and cell-to-cell communication. Plant Cell 14:5227–5238

    Google Scholar 

  • Kermicle JL (2001) Genetic barriers that restrict hybridization in corn and teosinte. Corn Sorghum Res Conf 56:17–23

    Google Scholar 

  • Kermicle JL, Allen JO (1990) Cross incompatibility between maize and teosinte. Maydica 35:399–408

    Google Scholar 

  • Lee EA, Darrah LL, Coe EH (1996) Dosage effects on morphological and quantitative traits in maize aneuploids. Genome 39:898–908

    Article  PubMed  CAS  Google Scholar 

  • Lewis D, Crowe LK (1958) Unilateral incompatibility in flowering plants. Heredity 12:233–256

    Google Scholar 

  • Liedl BE, McCormick S, Mutschler MA (1996) Unilateral incongruity in crosses involving Lycopersicon penellii and L. esculentum is distinct from self-incompatibility in expression, timing and location. Sex Plant Reprod 9:299–308

    Google Scholar 

  • Meyer P, Saedler H (1996) Homology-dependent gene silencing in plants. Annu Rev Plant Phys 47:23–48

    Article  CAS  Google Scholar 

  • Murfett J, Strabala TJ, Zurek DM, Mou B, Beecher B, McClure BA (1996) S RNase and interspecific pollen rejection in the genus Nicotiana: multiple pollen-rejection pathways contribute to unilateral incompatibility between self-incompatible and self-compatible species. Plant Cell 8:943–958

    Article  PubMed  CAS  Google Scholar 

  • Nelson OE (1952) Non-reciprocal cross-sterility in maize. Genetics 36:101–124

    Google Scholar 

  • Nelson OE (1993) The gametophyte factors of maize. In: Freeling M, Walbot V (eds) The maize handbook. Springer, Berlin Heidelberg New York pp 496–503

    Google Scholar 

  • Roman H (1947) Mitotic nondisjunction in the case of interchanges involving the B-type chromosome in maize. Genetics 32:391–409

    PubMed  CAS  Google Scholar 

  • Sanchez AM, Bosch M, Bots M, Nieuwland J, Feron R, Mariani C (2004) Pistil factors controlling pollination. Plant Cell 16:S98–S106

    Article  PubMed  CAS  Google Scholar 

  • Stone SL, Anderson EM, Mulen RT, Goring DR (2003) ARC1 is an E3 ubiquitin ligase and promotes the ubiquination of proteins during the rejection of self-incompatible Brassica pollen. Plant Cell 15:885–898

    Article  PubMed  Google Scholar 

  • Swanson R, Edlund AF, Preuss D (2004) Species specificity in pollen–pistil interactions. Annu Rev Genetics 38:739–818

    Google Scholar 

Download references

Acknowledgements

We thank Millard Susman for suggestions concerning the manuscript. Research supported by USDA NRI award 35301–13314.

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Correspondence to Jerry L. Kermicle.

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Kermicle, J.L., Evans, M.M. Pollen–pistil barriers to crossing in maize and teosinte result from incongruity rather than active rejection. Sex Plant Reprod 18, 187–194 (2005). https://doi.org/10.1007/s00497-005-0012-2

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  • DOI: https://doi.org/10.1007/s00497-005-0012-2

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