Molecular Breeding

, Volume 30, Issue 1, pp 239–250 | Cite as

Genetic linkage maps of the chromosomal regions associated with apomictic and sexual modes of reproduction in Cenchrus ciliaris

  • Chandra Bhan Yadav
  • Anuj
  • Suresh Kumar
  • M. G. Gupta
  • Vishnu Bhat
Article

Abstract

Cenchrus ciliaris reproduces by apomixis, an asexual mode of reproduction through seeds. Genetic analysis of apomixis in this species revealed that this trait is dominant and that a chromosomal region of more than 11 Mb controls this trait, which is hemizygous, heterochromatic and recombinationally suppressed. A novel F2 mapping population comprising 86 individuals segregating for apomictic and sexual modes of reproduction, generated after crossing a new set of obligate apomictic and sexual parents (IG-96-3108 and IG-96-443), was used in this study to identify a large number of amplified fragment length polymorphism (AFLP) and sequence characterized amplified region (SCAR) markers linked to these traits. Out of 180 polymorphic AFLP markers, 42 and 29 markers associated with apomixis and sexuality were mapped around Apo and Sexual loci, respectively. Markers 20G, 18G and 19G showed close linkage to Apo locus at map distance of only 1.1 cM, while 12FS, 4HS and 12b showed tight linkage to Sexual locus at map distance of 1.7 cM. Markers clustered around Apo and Sexual loci on either side. A large number of recombining AFLP markers were mapped around both loci, indicating a minor role of suppression of recombination. Four anchor markers from earlier studies also clustered around Apo locus, validating the present genetic linkage map. In addition, seven and one SCAR markers closely linked to Apo and Sexual loci were also developed, which could be used for fine mapping of the loci.

Keywords

Apomixis AFLP Genetic linkage map Sexual reproduction Cenchrus 

Notes

Acknowledgments

Authors wish to gratefully acknowledge the Department of Biotechnology, Govt. of India, New Delhi for the liberal funding to undertake a major part of the research work mentioned in this paper. We also wish to thank Director, IGFRI, Jhansi, UP, India for providing the plant material for research. We are grateful to Dr. Johan W. Van Ooijen, The Netherlands for helping us with data analysis for mapping using JoinMap software. We are grateful to the University of Delhi for the R&D grant to carry out part of this work. Authors are grateful to Dr. Avinash Kumar, T.H. Dar and Dr. Deepmala Sehgal for their help during the experimentation.

Supplementary material

11032_2011_9614_MOESM1_ESM.pptx (83 kb)
Linkage groups obtained for (a) male parent (IG-96-3108) and (b) female parent (IG-96-443) based on linkage analysis using JoinMap 2.0 software (PPTX 83 kb)

References

  1. Akiyama Y, Conner JA, Goel S, Morishige DT, Mullet JE, Hanna WW, Ozias-Akins P (2004) High-resolution physical mapping in Pennisetum squamulatum reveals extensive chromosomal heteromorphism of the genomic region associated with apomixis. Plant Physiol 134:1733–1741PubMedCrossRefGoogle Scholar
  2. Albertini E, Barcaccia G, Porceddu A, Sorbolini S, Falcinelli M (2001) Mode of reproduction is detected by Parth1 and Sex1 SCAR markers in a wide range of facultative apomictic Kentucky bluegrass varieties. Mol Breed 7:293–300CrossRefGoogle Scholar
  3. Bashaw EC (1962) Apomixis and sexuality in buffelgrass. Crop Sci 2:412–415CrossRefGoogle Scholar
  4. Bhat V, Dwivedi KK, Khurana JP, Sopory SK (2005) Apomixis: an enigma with potential applications. Curr Sci 89:1879–1893Google Scholar
  5. Bray RA (1978) Evidence for facultative apomixis in Cenchrus ciliaris. Euphytica 27:801–804CrossRefGoogle Scholar
  6. Catanach AS, Erasmuson SK, Podivinsky E, Jordan BR, Bicknell R (2006) Colloquium paper: deletion mapping of genetic regions associated with apomixis in Hieracium. Proc Natl Acad Sci USA 103:18650–18655PubMedCrossRefGoogle Scholar
  7. Dellaporta SL, Wood J, Hicks JB (1983) A plant DNA minipreparation: version II. Plant Mol Biol Rep 1:19–21CrossRefGoogle Scholar
  8. Dwivedi KK, Bhat BV, Gupta MG, Bhat SR, Bhat V (2007) Identification of a SCAR marker linked to apomixis in buffelgrass (Cenchrus ciliaris L.). Plant Sci 172:788–795CrossRefGoogle Scholar
  9. Ebina M, Nakagawa H, Yamamoto T, Araya H, Tsuruta S, Takahara M, Nakajima K (2005) Co-segregation of AFLP and RAPD markers to apospory in Guineagrass (Panicum maximum Jacq.). Grassland Sci 51:71–78CrossRefGoogle Scholar
  10. Fisher WD, Bashaw EC, Holt EC (1954) Evidence for apomixis in Pennisetum ciliare and Cenchrus setigerus. Agron J 46:401–410CrossRefGoogle Scholar
  11. Goel S, Chen Z, Conner JA, Akiyama Y, Hanna WW, Ozias-Akins P (2003) Physical evidence that a single hemizygous chromosomal region is sufficient to confer aposporous embryo sac formation in Pennisetum squamulatum and Cenchrus ciliaris. Genetics 163:1069–1082PubMedGoogle Scholar
  12. Goel S, Chen Z, Akiyama Y, Conner J, Basu M, Gualtieri G, Hanna W, Ozias-Akins P (2006) Comparative physical mapping of the apospory-specific genomic region in two apomictic grasses: Pennisetum squamulatum and Cenchrus ciliaris. Genetics 173:389–400PubMedCrossRefGoogle Scholar
  13. Grimanelli D, Leblanc O, Espinosa E, Perotti E, Gonzales de Leon D, Savidan Y (1998) Mapping diplosporous apomixis in tetraploid Tripsacum: one gene or several genes? Heredity 80:33–39PubMedCrossRefGoogle Scholar
  14. Gupta S, Gupta MG, Bhat BV, Bhat V (2001) Status of apomixis and sexuality in four species of Cenchrus. J Plant Biol 28:153–159Google Scholar
  15. Harlan JR, Brooks MH, Borgaonkar DSand DeWe JMJ (1964) Nature and inheritance of apomixis in Bothriochloa and Dichanthium. Bot Gaz 125:41–46CrossRefGoogle Scholar
  16. Huo H, Conner JA, Ozias-Akins P (2009) Genetic mapping of the apospory-specific genomic region in Pennisetum squamulatum using retrotransposon-based molecular markers. Theor Appl Genet 119:199–212PubMedCrossRefGoogle Scholar
  17. Jessup RW, Burson BL, Burow GB, Wang YW, Chang C, Li Z, Paterson AH, Hussey MA (2002) Disomic inheritance, suppressed recombination, and allelic interactions govern apospory in buffelgrass as revealed by genome mapping. Crop Sci 42:1688–1694CrossRefGoogle Scholar
  18. Labombarda P, Busti A, Caceres ME, Pupilli F, Arcioni S (2002) An AFLP marker tightly linked to apomixis reveals hemizygosity in a portion of the apomixis-controlling locus in Paspalum simplex. Genome 45:513–519PubMedCrossRefGoogle Scholar
  19. Matzk F, Prodanovic S, Bäumlein H, Schubert I (2005) The inheritance of apomixis in Poa pratensis confirms a five locus model with differences in gene expressivity and penetrance. Plant Cell 17:13–24PubMedCrossRefGoogle Scholar
  20. Noyes RD (2000) Diplospory and parthenogenesis in sexual × agamospermous (apomictic) Erigeron (Asteraceae) hybrids. Intl J Plant Sci 161:1–12CrossRefGoogle Scholar
  21. Ozias-Akins P (2006) Apomixis: developmental characteristics and genetics. Crit Rev Plant Sci 25:199–214CrossRefGoogle Scholar
  22. Ozias-Akins P, Van Dijk PJ (2007) Mendelian genetics of apomixis in plants. Annu Rev Genet 41:509–537PubMedCrossRefGoogle Scholar
  23. Ozias-Akins P, Roche D, Hanna WW (1998) Tight clustering and hemizygosity of apomixis-linked molecular markers in Pennisetum squamulatum implies genetic control of apospory by a divergent locus which may have no allelic form in sexual genotypes. Proc Natl Acad Sci USA 95:5127–5132PubMedCrossRefGoogle Scholar
  24. Pessino SC, Ortiz J, Leblanc O, do Valle CB, Hayward MD (1997) Identification of a maize linkage group related to apomixis in Brachiaria. Theor Appl Genet 94:439–444CrossRefGoogle Scholar
  25. Pessino SC, Evans C, Ortiz JPA, Armstead I, do Valle CB, Hayward MD (1998) A genetic map of the apospory-region in Brachiaria hybrids: identification of two markers closely associated with the trait. Hereditas 128:153–158CrossRefGoogle Scholar
  26. Porceddu P, Albertini E, Barcaccia G, Falistocco E, Falcinelli M (2002) Linkage mapping in apomictic and sexual bluegrass (Poa pratensis L.) genotypes using a two way pseudo-testcross strategy based on AFLP and SAMPL markers. Theor Appl Genet 104:273–280PubMedCrossRefGoogle Scholar
  27. Pupilli F, Labombarda P, Caceres ME, Quarin CL, Arcioni S (2001) The chromosome segment related to apomixis in Paspalum simplex is homoeologous to the telomeric region of the long arm of rice chromosome 12. Mol Breed 8:53–61CrossRefGoogle Scholar
  28. Roche D, Cong P, Chen ZB, Hanna WW, Gustine DL, Sherwood RT, Ozias-Akins P (1999) An apospory-specific genomic region is conserved between buffelgrass (Cenchrus ciliaris L.) and Pennisetum squamulatum Fresen. Plant J 19:203–208PubMedCrossRefGoogle Scholar
  29. Roche D, Chen Z, Hanna WW, Ozias-Akins P (2001) Non-Mendelian transmission of an apospory-specific genomic region in a reciprocal cross between sexual pearl millet (Pennisetum glaucum) and an apomictic F1 (P. glaucum × P. squamulatum). Sex Plant Reprod 13:217–223CrossRefGoogle Scholar
  30. Roche DR, Conner JA, Budiman MA, Frisch D, Wing R, Hanna WW, Ozias-Akins P (2002) Construction of BAC libraries from two apomictic grasses to study the microcolinearity of their aposporyspecific genomic regions. Theor Appl Genet 104:804–812PubMedCrossRefGoogle Scholar
  31. Schallau A, Arzenton F, Johnston AJ, Hähnel U, Koszegi D, Blattner FR, Altschmied L, Haberer G, Barcaccia G, Baumlein HW (2010) Identification and genetic analysis of the APOSPORY locus in Hypericum perforatum L. Plant J 62:773–784PubMedCrossRefGoogle Scholar
  32. Scott RJ (2007) Polyspermy in apomictic Crataegus: yes and no. New Phytol 173:227–229PubMedCrossRefGoogle Scholar
  33. Sehgal D, Rajpal VR, Raina SN, Sasanuma T, Sasakuma T (2009) Assaying polymorphism at DNA sequence level for new and novel genetic diversity diagnostics of the safflower (Carthamus tinctorius L.). Genetica 135:457–470PubMedCrossRefGoogle Scholar
  34. Sherwood RT, Young BA, Bashaw EC (1980) Facultative apomixis in buffelgrass. Bot Gaz 116:209–221Google Scholar
  35. Snyder LA, Hernandez Alice R, Warmke HE (1955) The mechanisms of apomixis in Pennisetum ciliare. Bot Gaz 116:209–221CrossRefGoogle Scholar
  36. Stam P, Van Ooijen JW (1995) JoinMap version 2.0: software for the calculation of genetic linkage maps. CPRO-DLO, Wageningen, The NetherlandsGoogle Scholar
  37. Stein J, Pessino SC, Martínez EJ, Rodriguez MP, Siena LA, Quarin CL, Ortiz JPA (2007) A genetic map of tetraploid Paspalum notatum Flügge (bahiagrass) based on single-dose molecular markers. Mol Breed 20:153–166CrossRefGoogle Scholar
  38. Tucker MR, Araujo ACG, Paech NA, Hecht V, Schmidt EDL, Rossel J-B, de Vries SC, Koltunow AM (2003) Sexual and apomictic reproduction in Hieracium subgenus Pilosella are closely interrelated developmental pathways. Plant Cell 15:1524–1537PubMedCrossRefGoogle Scholar
  39. Van Dijk PJ, Tas IC, Falque M, Bakx-Schotman T (1999) Crosses between sexual and apomictic dandelions (Taraxacum). II. The breakdown of apomixis. Heredity 83:715–721PubMedCrossRefGoogle Scholar
  40. Vijverberg K, Milanovic-Ivanovic S, Bakx-Schotman T, van Dijk PJ (2010) Genetic fine-mapping of DIPLOSPOROUS in Taraxacum (dandelion; Asteraceae) indicates a duplicated DIP-gene. BMC Plant Biol 10:154 (1-17)PubMedCrossRefGoogle Scholar
  41. Voorrips RE (2002) MapChart: software for the graphical presentation of linkage maps and QTLs. J Hered 93:77–78PubMedCrossRefGoogle Scholar
  42. Vos P, Hogers R, Bleeker M, Reijans M, Vandelee T, Hornes M, Frijters A, Pot J, Peleman J, Kuiper M, Zabeau M (1995) AFLP: A new technique for DNA fingerprinting. Nucleic Acids Res 23:4407–4414PubMedCrossRefGoogle Scholar
  43. Young BA, Sherwood RT, Bashaw EC (1979) Cleared-pistil and thicksectioning techniques for detecting aposporous apomixis in grasses. Can J Bot 57:1668–1672CrossRefGoogle Scholar
  44. Zorzatto C, Chiari L, De Araújo Bitencourt G, Do Valle CB, De Campos Leguizamón GO, Schuster I, Pagliarini MS (2010) Identification of a molecular marker linked to apomixis in Brachiaria humidicola (Poaceae). Plant Breed 129:734–736CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media B.V. 2011

Authors and Affiliations

  • Chandra Bhan Yadav
    • 1
  • Anuj
    • 1
  • Suresh Kumar
    • 2
    • 3
  • M. G. Gupta
    • 2
  • Vishnu Bhat
    • 1
  1. 1.Department of BotanyUniversity of DelhiDelhiIndia
  2. 2.Division of Crop ImprovementIndian Grassland and Fodder Research InstituteJhansiIndia
  3. 3.Department of Horticulture and Landscape ArchitecturePurdue UniversityWest LafayetteUSA

Personalised recommendations