Literature DB >> 8875863

Classification and phylogeny of the MADS-box multigene family suggest defined roles of MADS-box gene subfamilies in the morphological evolution of eukaryotes.

G Theissen1, J T Kim, H Saedler.   

Abstract

The MADS-box encodes a novel type of DNA-binding domain found so far in a diverse group of transcription factors from yeast, animals, and seed plants. Here, our first aim was to evaluate the primary structure of the MADS-box. Compilation of the 107 currently available MADS-domain sequences resulted in a signature which can strictly discriminate between genes possessing or lacking a MADS-domain and allowed a classification of MADS-domain proteins into several distinct subfamilies. A comprehensive phylogenetic analysis of known eukaryotic MADS-box genes, which is the first comprising animal as well as fungal and plant homologs, showed that the vast majority of subfamily members appear on distinct subtrees of phylogenetic trees, suggesting that subfamilies represent monophyletic gene clades and providing the proposed classification scheme with a sound evolutionary basis. A reconstruction of the history of the MADS-box gene subfamilies based on the taxonomic distribution of contemporary subfamily members revealed that each subfamily comprises highly conserved putative orthologs and recent paralogs. Some subfamilies must be very old (1,000 MY or more), while others are more recent. In general, subfamily members tend to share highly similar sequences, expression patterns, and related functions. The defined species distribution, specific function, and strong evolutionary conservation of the members of most subfamilies suggest that the establishment of different subfamilies was followed by rapid fixation and was thus highly advantageous during eukaryotic evolution. These gene subfamilies may have been essential prerequisites for the establishment of several complex eukaryotic body structures, such as muscles in animals and certain reproductive structures in higher plants, and of some signal transduction pathways. Phylogenetic trees indicate that after establishment of different subfamilies, additional gene duplications led to a further increase in the number of MADS-box genes. However, several molecular mechanisms of MADS-box gene diversification were used to a quite different extent during animal and plant evolution. Known plant MADS-domain sequences diverged much faster than those of animals, and gene duplication and sequence diversification were extensively used for the creation of new genes during plant evolution, resulting in a relatively large number of interacting genes. In contrast, the available data on animal genes suggest that increase in gene number was only moderate in the lineage leading to mammals, but in the case of MEF2-like gene products, heterodimerization between different splice variants may have increased the combinatorial possibilities of interactions considerably. These observations demonstrate that in metazoan and plant evolution, increased combinatorial possibilities of MADS-box gene product interactions correlated with the evolution of increasingly complex body plans.

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Year:  1996        PMID: 8875863     DOI: 10.1007/bf02337521

Source DB:  PubMed          Journal:  J Mol Evol        ISSN: 0022-2844            Impact factor:   2.395


  134 in total

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Authors:  Z Schwarz-Sommer; P Huijser; W Nacken; H Saedler; H Sommer
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2.  Two steps in the evolution of Antennapedia-class vertebrate homeobox genes.

Authors:  C Kappen; K Schughart; F H Ruddle
Journal:  Proc Natl Acad Sci U S A       Date:  1989-07       Impact factor: 11.205

3.  Functional interaction between the homeotic genes fbp1 and pMADS1 during petunia floral organogenesis.

Authors:  G C Angenent; M Busscher; J Franken; H J Dons; A J van Tunen
Journal:  Plant Cell       Date:  1995-05       Impact factor: 11.277

4.  Which is the most conserved group of proteins? Homology-orthology, paralogy, xenology, and the fusion of independent lineages.

Authors:  J P Gogarten
Journal:  J Mol Evol       Date:  1994-11       Impact factor: 2.395

Review 5.  Homeodomain proteins.

Authors:  W J Gehring; M Affolter; T Bürglin
Journal:  Annu Rev Biochem       Date:  1994       Impact factor: 23.643

6.  The yeast transcription activator PRTF, a homolog of the mammalian serum response factor, is encoded by the MCM1 gene.

Authors:  E E Jarvis; K L Clark; G F Sprague
Journal:  Genes Dev       Date:  1989-07       Impact factor: 11.361

7.  Manipulation of flower structure in transgenic tobacco.

Authors:  M A Mandel; J L Bowman; S A Kempin; H Ma; E M Meyerowitz; M F Yanofsky
Journal:  Cell       Date:  1992-10-02       Impact factor: 41.582

8.  Highly conserved residues in the bZIP domain of yeast GCN4 are not essential for DNA binding.

Authors:  W T Pu; K Struhl
Journal:  Mol Cell Biol       Date:  1991-10       Impact factor: 4.272

9.  Nucleotide sequences of novel potato (Solanum tuberosum L.) MADS-box cDNAs and their expression in vegetative organs.

Authors:  S G Kang; D J Hannapel
Journal:  Gene       Date:  1995-12-12       Impact factor: 3.688

10.  Bracteomania, an inflorescence anomaly, is caused by the loss of function of the MADS-box gene squamosa in Antirrhinum majus.

Authors:  P Huijser; J Klein; W E Lönnig; H Meijer; H Saedler; H Sommer
Journal:  EMBO J       Date:  1992-04       Impact factor: 11.598

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  140 in total

1.  Identification of a rice APETALA3 homologue by yeast two-hybrid screening.

Authors:  Y H Moon; J Y Jung; H G Kang; G An
Journal:  Plant Mol Biol       Date:  1999-05       Impact factor: 4.076

Review 2.  MADS about Gnetales.

Authors:  M W Frohlich
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-03       Impact factor: 11.205

3.  An ancestral MADS-box gene duplication occurred before the divergence of plants and animals.

Authors:  E R Alvarez-Buylla; S Pelaz; S J Liljegren; S E Gold; C Burgeff; G S Ditta; L Ribas de Pouplana; L Martínez-Castilla; M F Yanofsky
Journal:  Proc Natl Acad Sci U S A       Date:  2000-05-09       Impact factor: 11.205

Review 4.  Knots in the family tree: evolutionary relationships and functions of knox homeobox genes.

Authors:  L Reiser; P Sánchez-Baracaldo; S Hake
Journal:  Plant Mol Biol       Date:  2000-01       Impact factor: 4.076

Review 5.  Evolution of genes and taxa: a primer.

Authors:  J J Doyle; B S Gaut
Journal:  Plant Mol Biol       Date:  2000-01       Impact factor: 4.076

Review 6.  Progress in understanding angiosperm history, success, and relationships: Darwin's abominably "perplexing phenomenon".

Authors:  W L Crepet
Journal:  Proc Natl Acad Sci U S A       Date:  2000-11-21       Impact factor: 11.205

7.  Identification and characterization of three orchid MADS-box genes of the AP1/AGL9 subfamily during floral transition.

Authors:  H Yu; C J Goh
Journal:  Plant Physiol       Date:  2000-08       Impact factor: 8.340

8.  Cloning, mapping and expression analysis of barley MADS-box genes.

Authors:  J Schmitz; R Franzen; T H Ngyuen; F Garcia-Maroto; C Pozzi; F Salamini; W Rohde
Journal:  Plant Mol Biol       Date:  2000-04       Impact factor: 4.076

9.  Spatial and temporal expression of the orchid floral homeotic gene DOMADS1 is mediated by its upstream regulatory regions.

Authors:  Hao Yu; Shu Hua Yang; Chong Jin Goh
Journal:  Plant Mol Biol       Date:  2002-05       Impact factor: 4.076

10.  Molecular genetics of ecological diversification: duplication and rapid evolution of toxin genes of the venomous gastropod Conus.

Authors:  T F Duda; S R Palumbi
Journal:  Proc Natl Acad Sci U S A       Date:  1999-06-08       Impact factor: 11.205

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