The confirmation of putative natural hybrid species Meconopsis × cookei G. Taylor (papaveraceae) based on nuclear ribosomal DNA ITS region sequence

Acta Genetica Sinica

Volumn 31, Issue 9, 2004, Pages 901-907

  Yuan, Chang Chun ^a   Li, Pei Xin ^a   Wang, Yan Fang ^a   Shi, Su Hua ^b  

^a LINGNAN NORMAL UNIVERSITY   (China)

^b SUN YAT SEN UNIVERSITY   (China)

Author keywords

Hybrid species; ITS; M. punicea; M. quintuplinervia; Meconopsis cookei

Indexed keywords

INTERNAL TRANSCRIBED SPACER; RIBOSOME DNA;

ARTICLE; COMPUTER PROGRAM; GENE LOCUS; HYBRID; MECONOPSIS PUNICEA; MECONOPSIS QUINTUPLINERVIA; MECONOPSIS X COOKEI; NONHUMAN; NUCLEOTIDE SEQUENCE; PAPAVERACEAE; SEQUENCE ALIGNMENT;

BASE SEQUENCE; CHIMERA; DNA, RIBOSOMAL SPACER; MOLECULAR SEQUENCE DATA; PAPAVERACEAE;

EMBRYOPHYTA; MECONOPSIS; PAPAVERACEAE;

EID: 8444230989     PISSN: 03794172     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (21)

1. Taylor G. Two new Meconopsis hybrids, Journ Roy Hort Soc, 1951, 126:231-232.
2. Cobb J L S. Meconopsis. Portland, Oregon: Timber Press, 1989, 1-125.
3. Soltis D E, Soltis P S. Molecular data and the dynamic nature of polyploidy. Critical Reviews in Plant Sciences, 1993, 12:243-273.
4. Rieseberg L H. The role of hybridization in evolution: old wine in new skins. American Journal of Botany, 1995, 82: 944-953.
5. Rauscher J T, Doyle J J, Brown A H D. Internal transcribed spacer repeat-specific primers and the analysis of hybridization in the Glycine tomentella (Leguminosae) polyploid complex. Molecular Ecology, 2002, 11(12):2691-2702.
6. Soltis P S, Doyle J J, Sortis D E. Molecular data and polyploid evolution in plants. In: Soltis P S, Soltis D E, Doyle J J, eds. Molecular Systematics of Plants. New York: Chapman & Hall, 1992, 177-201.
7. Quijada A, Liston A, Robinson W, AlvarezBuylla E. The ribosomal ITS region as a marker to detect hybridization in pines. Molecular Ecology, 1997, 6:995-996.
8. Sang T, Crawford D J, Stuessy T F. Documentation of reticulate evolution in peonies (Peonia) using internal transcribed spacer sequences of nuclear ribosomal DNA: implications for biogeography and concerted evolution. Proceedings of the National Academy of Sciences of the United States of America, 1995, 92:6813-6817.
9. Baldwin B G. Phylogenetic utility of the internal transcribed spacers of nuclear ribosomal DNA in plants: an example from the Compositae. Molecular Phylogenetics and Evolution, 1992, 1:3-16.
10. Baldwin B G, Sanderson M J, Porter J M, Wojciechowski M F, Campbell C S, Donoghue M J. The ITS region of nuclear ribosomal DNA: a valuable source of evidence on angiosperm phytogeny. Ann Missouri Bot Gard. 1995, 82:247-277.
11. Rogers S O, Bendich A J. Ribosomal RNA genes in plants: variability in copy number and in the intergenic spacer. Plant Mol Biol, 1987, 9:509-520.
12. WANG Jian-Bo, ZHANG Wen-Ju, CHEN Jia-Kuan. Application of ITS sequences of nuclear rDNA in phylogenetic and evolutionary studies of angiosperms. Acta Phytotaxonomica Sinica, 1999, 37(4):407-416.
13. Doyle J, Doyle J L. A rapid DNA isolation method for small quantities of fresh tissues. Phytochem Bull, 1987, 19:11-15.
14. White T J, Bruns T, Lee S, Taylor J. Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenies. In: Innis M A, Gelfand D H, Sninsky J J, White T J, eds. PCR Protocols. San Diego: Academic Press, 1990, 315-322.
15. Emshwiller E, Doyle J J. Origins of domestication and polyploidy in oca (Oxalis tuberosa: Oxalidaceae): nrDNA ITS data. American Journal of Botany, 1998, 85:975-985.
16. Franzke A, Mummenhoff K. Recent hybrid speciation in Cardamine (Brassicaceae) conversion of nuclear ribosomal ITS sequences in statu nascendi. Theoretical and Applied Genetics, 1999, 98:831-834.
17. Vargas P, McAllister H A, Morton C, Jury S L, Wilkinson M J. Polyploid speciation in Hedera (Araliaceae): phylogenetic and biogeographic insights based on chromosome counts and ITS sequences. Plant Systematics and Evolution, 1999, 219:165-179.
18. Widmer A, Baltisberger M. Molecular evidence for allopolyploid speciation and a single origin of the narrow endemic Draba Iadina (Brassicaceae). American Journal of Botany, 1999, 86:1282-1289.
19. Whittall J, Liston A, Gisler S, Meinke R J. Detecting nucelotide additivity from direct sequences is a SNAP: an example from Sidalcea (Malvaceae). Plant Biology, 2000, 2: 211-217.
20. Hodkinson T R, Chase M W, Takahashi C. The use of DNA sequencing (ITS and TrnL-F), AFLP, and fluorescent in situ hybridization to study allopolyploid Miscanthus (Poaceae). American Journal of Bofany, 2002, 89:279-286.
21. Hardig T M, Soltis P S, Soltis D E, Hudson R B. Morphological and molecular analysis of putative hybrid speciation in Ceanothus (Rhamnaceae). Systematic Botany, 2002, 27 (4):734-746.