Phenotypic plasticity of aposporous embryo sac development in Hieracium praealtum

References

• Yadegari R, Drews GN. Female gametophyte development. Plant Cell. 2004;16:S133–S141. doi:10.1105/tpc.018192.
   PubMed Web of Science ®Google Scholar
• Carman JG. Asynchronous expression of duplicate genes in angiosperms may cause apomixis, bispory, tetraspory, and polyembryony. Bio J Linnean Soc. 1997;61:51–94. doi:10.1111/j.1095-8312.1997.tb01778.x.
   Web of Science ®Google Scholar
• Hojsgaard D, Klatt S, Baier R, Carman JG, Horandl E. Taxonomy and Biogeography of Apomixis in Angiosperms and Associated Biodiversity Characteristics. CRC Crit Rev Plant Sci. 2014;33:414–427. doi:10.1080/07352689.2014.898488.
   PubMed Web of Science ®Google Scholar
• Naumova T. Apomixis in Angiosperms: nucellar and integumentary embryony, Ed 1st. Boca Raton (FL, USA): CRC Press; 1993.
   Google Scholar
• Zhang SQ, Liang M, Wang N, Xu Q, Deng XX, Chai LJ. Reproduction in woody perennial Citrus: an update on nucellar embryony and self-incompatibility. Plant Reprod. 2018;31:43–57. doi:10.1007/s00497-018-0327-4.
   PubMed Web of Science ®Google Scholar
• Catanach AS, Erasmuson SK, Podivinsky E, Jordan BR, Bicknell R. Deletion mapping of genetic regions associated with apomixis in Hieracium. Proc Natl Acad Sci USA. 2006;103:18650–18655. doi:10.1073/pnas.0605588103.
   PubMed Web of Science ®Google Scholar
• Koltunow AMG, Johnson SD, Rodrigues JCM, Okada T, Hu YK, Tsuchiya T, Wilson S, Fletcher P, Ito K, Suzuki G, et al. Sexual reproduction is the default mode in apomictic Hieracium subgenus Pilosella, in which two dominant loci function to enable apomixis. Plant J. 2011;66:890–902. doi:10.1111/j.1365-313X.2011.04556.x.
   PubMed Web of Science ®Google Scholar
• Okada T, Hu YK, Tucker MR, Taylor JM, Johnson SD, Spriggs A, Tsuchiya T, Oelkers K, Rodrigues JCM, Koltunow AMG. Enlarging cells initiating apomixis in Hieracium praealtum transition to an embryo sac program prior to entering mitosis. Plant Physiol. 2013;163:216–231. doi:10.1104/pp.113.219485.
   PubMed Web of Science ®Google Scholar
• Rabiger DS, Taylor JM, Spriggs A, Hand ML, Henderson ST, Johnson SD, Oelkers K, Hrmova M, Saito K, Suzuki G, et al. Generation of an integrated Hieracium genomic and transcriptomic resource enables exploration of small RNA pathways during apomixis initiation. BMC Biol. 2016;14. doi:10.1186/s12915-016-0311-0.
   PubMed Web of Science ®Google Scholar
• Bräuning S, Catanach A, Lord JM, Bicknell R, Macknight RC. Comparative transcriptome analysis of the wild-type model apomict Hieracium praealtum and its loss of parthenogenesis (lop) mutant. BMC Plant Biol. 2018;18:206. doi:10.1186/s12870-018-1423-1.
   PubMed Web of Science ®Google Scholar
• Juranić M, Tucker MR, Schultz CJ, Shirley NJ, Taylor JM, Spriggs A, Johnson SD, Bulone V, Koltunow AM. Asexual female gametogenesis involves contact with a sexually-fated megaspore in apomictic Hieracium. Plant Physiol. 2018;177:1027–1049. doi:10.1104/pp.18.00342.
   PubMed Web of Science ®Google Scholar
• Okada T, Ito K, Johnson SD, Oelkers K, Suzuki G, Houben A, Mukai Y, Koltunow AM. Chromosomes carrying meiotic avoidance loci in three apomictic eudicot Hieracium subgenus Pilosella species share structural features with two monocot apomicts. Plant Physiol. 2011;157:1327–1341. doi:10.1104/pp.111.181164.
   PubMed Web of Science ®Google Scholar
• Koltunow AM, Johnson SD, Bicknell RA. Apomixis is not developmentally conserved in related, genetically characterized Hieracium plants of varying ploidy. Sex Plant Reprod. 2000;12:253–266. doi:10.1007/s004970050193.
   Google Scholar
• Koltunow AM, Johnson SD, Bicknell RA. Sexual and apomictic development in Hieracium. Sex Plant Reprod. 1998;11:213–230. doi:10.1007/s004970050144.
   Google Scholar
• Bicknell RA, Lambie SC, Butler RC. Quantification of progeny classes, in two facultatively apotnictic accessions of Hieracium. Hereditas. 2003;138:11–20.
   PubMed Web of Science ®Google Scholar
• Nakagawa H. Embryo sac analysis and crossing procedure for breeding apomictic guineagrass (panicum-maximum jacq). Jarq-Jpn Agr Res Q. 1990;24:163–168.
   Google Scholar
• Albertini E, Porceddu A, Ferranti F, Reale L, Barcaccia G, Romano B, Falcinelli M. Apospory and parthenogenesis may be uncoupled in Poa pratensis: a cytological investigation. Sex Plant Reprod. 2001;14:213–217. doi:10.1007/s00497-001-0116-2.
   PubMedGoogle Scholar
• Ozias-Akins P. Apomixis: Developmental characteristics and genetics. CRC Crit Rev Plant Sci. 2006;25:199–214. doi:10.1080/07352680600563926.
   Web of Science ®Google Scholar
• Hojsgaard DH, Martinez EJ, Quarin CL. Competition between meiotic and apomictic pathways during ovule and seed development results in clonality. New Phytol. 2013;197:336–347. doi:10.1111/j.1469-8137.2012.04381.x.
   PubMed Web of Science ®Google Scholar
• Rios E, Kenworthy K, Blount A, Quesenberry K, Unruh B, Erickson J, Altpeter F, Munoz P. Breeding apomictic bahiagrass (Paspalum notatum Flugge) with improved turf traits. Plant Breed. 2017;136:253–260. doi:10.1111/pbr.12459.
   Web of Science ®Google Scholar
• Yudakova OI, Shakina TN. Specific features of early embryogenesis in apomictic Poa pratensis L. Russ J Dev Biol. 2007;38:1–6. doi:10.1134/S1062360407010018.
   Google Scholar
• Chen L, Guan L. Ultrastructural mechanisms of aposporous embryo sac initial cell appearance and its developmental process in gametophytic apomicts of guinea grass (panicum maximum). In The Transmission Electron Microscope, editor. Maaz K, IntechOpen (London, UK), 2012;233. doi:10.5772/34912.
   Google Scholar