Literature DB >> 11673632

A MADS box gene from lily (Lilium Longiflorum) is sufficient to generate dominant negative mutation by interacting with PISTILLATA (PI) in Arabidopsis thaliana.

T Y Tzeng1, C H Yang.   

Abstract

Lily MADS box gene 1 (LMADS1), with sequence homology to the AP3 family of genes, was cloned and characterized from lily (Lilium longiflorum). LMADS1 protein contains almost complete consensus sequence of the PISTILLATA (PI)-derived motif (YEFRVQPSQPNLH) found in the AP3 family of genes and paleoAP3 motif (YGSHDLRLA) found in the AP3 family of genes from the low eudicot, magnolid dicot and monocot species. LMADS1 mRNA was expressed in all four whorls of the flower and absent in the vegetative leaves. The LMADS1 protein was only detected in the petals and stamens, indicating that LMADS1 is possibly post-transcriptionally regulated in lily. Arabidopsis plants transformed with 35S::LMADS1 produced flowers with short petals and stamens, however, no floral organ conversion was observed. Ectopic expression of LMADS1 cDNA truncated with the MADS box domain in Arabidopsis generated the ap3-like dominant negative mutation in which the petals were converted into sepal-like structures and the stamens were converted into carpel-like structures. Yeast two-hybrid analysis indicated that LMADS1 truncated with the MADS box domain is able to sufficiently interact with the Arabidopsis PI protein. This result supports that LMADS1 is the functional counterpart of the AP3 gene in lily. Interestingly, in contrast to other B functional genes, LMADS1 truncated with the MADS box domain is able to strongly form homodimers. LMADS1 may represent an ancestral form of the B function gene, which retains the ability to form homodimers in regulating petal and stamen development in lily.

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Year:  2001        PMID: 11673632     DOI: 10.1093/pcp/pce151

Source DB:  PubMed          Journal:  Plant Cell Physiol        ISSN: 0032-0781            Impact factor:   4.927


  32 in total

1.  Analysis of the petunia MADS-box transcription factor family.

Authors:  R G H Immink; S Ferrario; J Busscher-Lange; M Kooiker; M Busscher; G C Angenent
Journal:  Mol Genet Genomics       Date:  2003-01-15       Impact factor: 3.291

2.  Ectopic expression of carpel-specific MADS box genes from lily and lisianthus causes similar homeotic conversion of sepal and petal in Arabidopsis.

Authors:  Tsai-Yu Tzeng; Hsing-Yu Chen; Chang-Hsien Yang
Journal:  Plant Physiol       Date:  2002-12       Impact factor: 8.340

3.  Two lily SEPALLATA-like genes cause different effects on floral formation and floral transition in Arabidopsis.

Authors:  Tsai-Yu Tzeng; Chih-Chi Hsiao; Pei-Ju Chi; Chang-Hsien Yang
Journal:  Plant Physiol       Date:  2003-10-02       Impact factor: 8.340

4.  Heterotopic expression of class B floral homeotic genes supports a modified ABC model for tulip (Tulipa gesneriana).

Authors:  Akira Kanno; Hiroshi Saeki; Toshiaki Kameya; Heinz Saedler; Günter Theissen
Journal:  Plant Mol Biol       Date:  2003-07       Impact factor: 4.076

5.  Morphological alterations by ectopic expression of the rice OsMADS4 gene in tobacco plants.

Authors:  Hong-Gyu Kang; Gynheung An
Journal:  Plant Cell Rep       Date:  2005-02-10       Impact factor: 4.570

6.  Elaboration of B gene function to include the identity of novel floral organs in the lower eudicot Aquilegia.

Authors:  Elena M Kramer; Lynn Holappa; Billie Gould; M Alejandra Jaramillo; Dimitriy Setnikov; Philip M Santiago
Journal:  Plant Cell       Date:  2007-03-30       Impact factor: 11.277

7.  FOREVER YOUNG FLOWER Negatively Regulates Ethylene Response DNA-Binding Factors by Activating an Ethylene-Responsive Factor to Control Arabidopsis Floral Organ Senescence and Abscission.

Authors:  Wei-Han Chen; Pei-Fang Li; Ming-Kun Chen; Yung-I Lee; Chang-Hsien Yang
Journal:  Plant Physiol       Date:  2015-06-10       Impact factor: 8.340

Review 8.  Lily breeding by using molecular tools and transformation systems.

Authors:  Xiaohua Liu; Jiahui Gu; Jingmao Wang; Yingmin Lu
Journal:  Mol Biol Rep       Date:  2014-07-19       Impact factor: 2.316

9.  Characterization of the possible roles for B class MADS box genes in regulation of perianth formation in orchid.

Authors:  Yu-Yun Chang; Nai-Hsuan Kao; Jen-Ying Li; Wei-Han Hsu; Yu-Ling Liang; Jia-Wei Wu; Chang-Hsien Yang
Journal:  Plant Physiol       Date:  2009-12-16       Impact factor: 8.340

10.  Environmental control of sepalness and petalness in perianth organs of waterlilies: a new Mosaic theory for the evolutionary origin of a differentiated perianth.

Authors:  Kate A Warner; Paula J Rudall; Michael W Frohlich
Journal:  J Exp Bot       Date:  2009-07-02       Impact factor: 6.992

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