Literature DB >> 21527418

A double-flowered variety of lesser periwinkle (Vinca minor fl. pl.) that has persisted in the wild for more than 160 years.

Yong-Qiang Wang1, Rainer Melzer, Günter Theissen.   

Abstract

BACKGROUND AND AIMS: Homeotic transitions are usually dismissed by population geneticists as credible modes of evolution due to their assumed negative impact on fitness. However, several lines of evidence suggest that such changes in organ identity have played an important role during the origin and subsequent evolution of the angiosperm flower. Better understanding of the performance of wild populations of floral homeotic varieties should help to clarify the evolutionary potential of homeotic mutants. Wild populations of plants with changes in floral symmetry, or with reproductive organs replacing perianth organs or sepals replacing petals have already been documented. However, although double-flowered varieties are quite popular as ornamental and garden plants, they are rarely found in the wild and, if they are, usually occur only as rare mutant individuals, probably because of their low fitness relative to the wild-type. We therefore investigated a double-flowered variety of lesser periwinkle, Vinca minor flore pleno (fl. pl.), that is reported to have existed in the wild for at least 160 years. To assess the merits of this plant as a new model system for investigations on the evolutionary potential of double-flowered varieties we explored the morphological details and distribution of the mutant phenotype.
METHODS: The floral morphology of the double-flowered variety and of a nearby population of wild-type plants was investigated by means of visual inspection and light microscopy of flowers, the latter involving dissected or sectioned floral organs. KEY
RESULTS: The double-flowered variety was found in several patches covering dozens of square metres in a forest within the city limits of Jena (Germany). It appears to produce fewer flowers than the wild-type, and its flowers are purple rather than blue. Most sepals in the first floral whorl resemble those in the wild-type, although occasionally one sepal is broadened and twisted. The structure of second-whorl petals is very similar to that of the wild-type, but their number per flower is more variable. The double-flowered character is due to partial or complete transformation of stamens in the third whorl into petaloid organs. Occasionally, 'flowers within flowers' also develop on elongated pedicels in the double-flowered variety.
CONCLUSIONS: The flowers of V. minor fl. pl. show meristic as well as homeotic changes, and occasionally other developmental abnormalities such as mis-shaped sepals or loss of floral determinacy. V. minor fl. pl. thus adds to a growing list of natural floral homeotic varieties that have established persistent populations in the wild. Our case study documents that even mutant varieties that have reproductive organs partially transformed into perianth organs can persist in the wild for centuries. This finding makes it at least conceivable that even double-flowered varieties have the potential to establish new evolutionary lineages, and hence may contribute to macroevolutionary transitions and cladogenesis.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21527418      PMCID: PMC3108809          DOI: 10.1093/aob/mcr090

Source DB:  PubMed          Journal:  Ann Bot        ISSN: 0305-7364            Impact factor:   4.357


  30 in total

Review 1.  Development of floral organ identity: stories from the MADS house.

Authors:  G Theissen
Journal:  Curr Opin Plant Biol       Date:  2001-02       Impact factor: 7.834

Review 2.  The proper place of hopeful monsters in evolutionary biology.

Authors:  Günter Theissen
Journal:  Theory Biosci       Date:  2005-12-20       Impact factor: 1.919

3.  A conserved microRNA module exerts homeotic control over Petunia hybrida and Antirrhinum majus floral organ identity.

Authors:  Maria Cartolano; Rosa Castillo; Nadia Efremova; Markus Kuckenberg; Jan Zethof; Tom Gerats; Zsuzsanna Schwarz-Sommer; Michiel Vandenbussche
Journal:  Nat Genet       Date:  2007-06-24       Impact factor: 38.330

4.  Saltational evolution: hopeful monsters are here to stay.

Authors:  Günter Theissen
Journal:  Theory Biosci       Date:  2009-02-18       Impact factor: 1.919

5.  The protein encoded by the Arabidopsis homeotic gene agamous resembles transcription factors.

Authors:  M F Yanofsky; H Ma; J L Bowman; G N Drews; K A Feldmann; E M Meyerowitz
Journal:  Nature       Date:  1990-07-05       Impact factor: 49.962

6.  Floral homeotic mutations produced by transposon-mutagenesis in Antirrhinum majus.

Authors:  R Carpenter; E S Coen
Journal:  Genes Dev       Date:  1990-09       Impact factor: 11.361

7.  Co-suppression of the petunia homeotic gene fbp2 affects the identity of the generative meristem.

Authors:  G C Angenent; J Franken; M Busscher; D Weiss; A J van Tunen
Journal:  Plant J       Date:  1994-01       Impact factor: 6.417

8.  Conservation and divergence in the AGAMOUS subfamily of MADS-box genes: evidence of independent sub- and neofunctionalization events.

Authors:  Laura M Zahn; James H Leebens-Mack; Jennifer M Arrington; Yi Hu; Lena L Landherr; Claude W dePamphilis; Annette Becker; Günter Theissen; Hong Ma
Journal:  Evol Dev       Date:  2006 Jan-Feb       Impact factor: 1.930

9.  Control of floral homeotic gene expression and organ morphogenesis in Antirrhinum.

Authors:  P C McSteen; C A Vincent; S Doyle; R Carpenter; E S Coen
Journal:  Development       Date:  1998-07       Impact factor: 6.868

10.  Complementary floral homeotic phenotypes result from opposite orientations of a transposon at the plena locus of Antirrhinum.

Authors:  D Bradley; R Carpenter; H Sommer; N Hartley; E Coen
Journal:  Cell       Date:  1993-01-15       Impact factor: 41.582

View more
  7 in total

Review 1.  Development and evolution of extreme synorganization in angiosperm flowers and diversity: a comparison of Apocynaceae and Orchidaceae.

Authors:  Peter K Endress
Journal:  Ann Bot       Date:  2015-08-20       Impact factor: 4.357

2.  Isolation of a CENTRORADIALIS/TERMINAL FLOWER1 homolog in saffron (Crocus sativus L.): characterization and expression analysis.

Authors:  Athanasios Tsaftaris; Konstantinos Pasentsis; Apostolos Kalivas; Sofia Michailidou; Panagiotis Madesis; Anagnostis Argiriou
Journal:  Mol Biol Rep       Date:  2012-04-26       Impact factor: 2.316

3.  The evolution of flower development: current understanding and future challenges.

Authors:  Annette Becker; Karine Alix; Catherine Damerval
Journal:  Ann Bot       Date:  2011-06       Impact factor: 4.357

Review 4.  Genetics and genomics of flower initiation and development in roses.

Authors:  Mohammed Bendahmane; Annick Dubois; Olivier Raymond; Manuel Le Bris
Journal:  J Exp Bot       Date:  2013-01-29       Impact factor: 6.992

5.  Loss of deeply conserved C-class floral homeotic gene function and C- and E-class protein interaction in a double-flowered ranunculid mutant.

Authors:  Kelsey D Galimba; Theadora R Tolkin; Alessandra M Sullivan; Rainer Melzer; Günter Theißen; Verónica S Di Stilio
Journal:  Proc Natl Acad Sci U S A       Date:  2012-08-01       Impact factor: 11.205

6.  Dosage imbalance of B- and C-class genes causes petaloid-stamen relating to F1 hybrid variation.

Authors:  Jing Liu; Chao-Qun Li; Yang Dong; Xia Yang; Yin-Zheng Wang
Journal:  BMC Plant Biol       Date:  2018-12-07       Impact factor: 4.215

Review 7.  Evolution of unusual morphologies in Lentibulariaceae (bladderworts and allies) and Podostemaceae (river-weeds): a pictorial report at the interface of developmental biology and morphological diversification.

Authors:  Rolf Rutishauser
Journal:  Ann Bot       Date:  2015-11-20       Impact factor: 4.357

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.