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2.
Nature ; 449(7161): 463-7, 2007 Sep 27.
Article in English | MEDLINE | ID: mdl-17721507

ABSTRACT

The analysis of the first plant genomes provided unexpected evidence for genome duplication events in species that had previously been considered as true diploids on the basis of their genetics. These polyploidization events may have had important consequences in plant evolution, in particular for species radiation and adaptation and for the modulation of functional capacities. Here we report a high-quality draft of the genome sequence of grapevine (Vitis vinifera) obtained from a highly homozygous genotype. The draft sequence of the grapevine genome is the fourth one produced so far for flowering plants, the second for a woody species and the first for a fruit crop (cultivated for both fruit and beverage). Grapevine was selected because of its important place in the cultural heritage of humanity beginning during the Neolithic period. Several large expansions of gene families with roles in aromatic features are observed. The grapevine genome has not undergone recent genome duplication, thus enabling the discovery of ancestral traits and features of the genetic organization of flowering plants. This analysis reveals the contribution of three ancestral genomes to the grapevine haploid content. This ancestral arrangement is common to many dicotyledonous plants but is absent from the genome of rice, which is a monocotyledon. Furthermore, we explain the chronology of previously described whole-genome duplication events in the evolution of flowering plants.


Subject(s)
Evolution, Molecular , Genome, Plant/genetics , Polyploidy , Vitis/classification , Vitis/genetics , Arabidopsis/genetics , DNA, Intergenic/genetics , Exons/genetics , Genes, Plant/genetics , Introns/genetics , Karyotyping , MicroRNAs/genetics , Molecular Sequence Data , Oryza/genetics , Populus/genetics , RNA, Plant/genetics , RNA, Transfer/genetics , Sequence Analysis, DNA
3.
Nature ; 421(6923): 601-7, 2003 Feb 06.
Article in English | MEDLINE | ID: mdl-12508121

ABSTRACT

Chromosome 14 is one of five acrocentric chromosomes in the human genome. These chromosomes are characterized by a heterochromatic short arm that contains essentially ribosomal RNA genes, and a euchromatic long arm in which most, if not all, of the protein-coding genes are located. The finished sequence of human chromosome 14 comprises 87,410,661 base pairs, representing 100% of its euchromatic portion, in a single continuous segment covering the entire long arm with no gaps. Two loci of crucial importance for the immune system, as well as more than 60 disease genes, have been localized so far on chromosome 14. We identified 1,050 genes and gene fragments, and 393 pseudogenes. On the basis of comparisons with other vertebrate genomes, we estimate that more than 96% of the chromosome 14 genes have been annotated. From an analysis of the CpG island occurrences, we estimate that 70% of these annotated genes are complete at their 5' end.


Subject(s)
Chromosomes, Human, Pair 14/genetics , Physical Chromosome Mapping , Sequence Analysis, DNA , 5' Untranslated Regions/genetics , Animals , Base Composition , Chromosomes, Artificial/genetics , CpG Islands/genetics , DNA, Mitochondrial/genetics , DNA, Ribosomal/genetics , Genes/genetics , Genomics , Humans , Immunity/genetics , Mice , Microsatellite Repeats/genetics , Molecular Sequence Data , Open Reading Frames/genetics , Pseudogenes/genetics , Reproducibility of Results , Synteny/genetics
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