111
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      A Map-Based Cloning Strategy Employing a Residual Heterozygous Line Reveals that the GIGANTEA Gene Is Involved in Soybean Maturity and Flowering

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Flowering is indicative of the transition from vegetative to reproductive phase, a critical event in the life cycle of plants. In soybean ( Glycine max), a flowering quantitative trait locus, FT2, corresponding to the maturity locus E2, was detected in recombinant inbred lines (RILs) derived from the varieties “Misuzudaizu” ( ft2/ft2; JP28856) and “Moshidou Gong 503” ( FT2/FT2; JP27603). A map-based cloning strategy using the progeny of a residual heterozygous line (RHL) from the RIL was employed to isolate the gene responsible for this quantitative trait locus. A GIGANTEA ortholog, GmGIa (Glyma10g36600), was identified as a candidate gene. A common premature stop codon at the 10th exon was present in the Misuzudaizu allele and in other near isogenic lines (NILs) originating from Harosoy ( e2/e2; PI548573). Furthermore, a mutant line harboring another premature stop codon showed an earlier flowering phenotype than the original variety, Bay ( E2/E2; PI553043). The e2/e2 genotype exhibited elevated expression of GmFT2a, one of the florigen genes that leads to early flowering. The effects of the E2 allele on flowering time were similar among NILs and constant under high (43°N) and middle (36°N) latitudinal regions in Japan. These results indicate that GmGIa is the gene responsible for the E2 locus and that a null mutation in GmGIa may contribute to the geographic adaptation of soybean.

          Related collections

          Most cited references50

          • Record: found
          • Abstract: found
          • Article: not found
          Is Open Access

          The grapevine genome sequence suggests ancestral hexaploidization in major angiosperm phyla.

          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.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Rapid isolation of high molecular weight plant DNA.

            A method is presented for the rapid isolation of high molecular weight plant DNA (50,000 base pairs or more in length) which is free of contaminants which interfere with complete digestion by restriction endonucleases. The procedure yields total cellular DNA (i.e. nuclear, chloroplast, and mitochondrial DNA). The technique is ideal for the rapid isolation of small amounts of DNA from many different species and is also useful for large scale isolations.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              AFLP: a new technique for DNA fingerprinting.

              A novel DNA fingerprinting technique called AFLP is described. The AFLP technique is based on the selective PCR amplification of restriction fragments from a total digest of genomic DNA. The technique involves three steps: (i) restriction of the DNA and ligation of oligonucleotide adapters, (ii) selective amplification of sets of restriction fragments, and (iii) gel analysis of the amplified fragments. PCR amplification of restriction fragments is achieved by using the adapter and restriction site sequence as target sites for primer annealing. The selective amplification is achieved by the use of primers that extend into the restriction fragments, amplifying only those fragments in which the primer extensions match the nucleotides flanking the restriction sites. Using this method, sets of restriction fragments may be visualized by PCR without knowledge of nucleotide sequence. The method allows the specific co-amplification of high numbers of restriction fragments. The number of fragments that can be analyzed simultaneously, however, is dependent on the resolution of the detection system. Typically 50-100 restriction fragments are amplified and detected on denaturing polyacrylamide gels. The AFLP technique provides a novel and very powerful DNA fingerprinting technique for DNAs of any origin or complexity.
                Bookmark

                Author and article information

                Contributors
                Role: Communicating editor
                Journal
                Genetics
                genetics
                genetics
                genetics
                Genetics
                Genetics Society of America
                0016-6731
                1943-2631
                June 2011
                June 2011
                June 2011
                : 188
                : 2
                : 395-407
                Affiliations
                [* ]National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8602, Japan,
                []Northeast Institute of Geography and Agroecology, Chinese Academy of Sciences, Harbin 150040, People's Republic of China,
                []Faculty of Agriculture, Saga University, Saga 840-8502, Japan,
                [§ ]Kazusa DNA Research Institute, Kisarazu, Chiba 292-0812, Japan,
                [** ]Japan International Research Center for Agricultural Sciences, Tsukuba, Ibaraki 305-8686, Japan,
                [†† ]National Institute of Crop Science, Tsukuba, Ibaraki 305-8518, Japan and
                [‡‡ ]Graduate School of Agriculture, Hokkaido University, Sapporo, Hokkaido 060-8589, Japan
                Author notes

                Supporting information is available online at http://www.genetics.org/cgi/content/full/genetics.110.125062/DC1.

                Sequence data described in this article have been deposited at the DNA Data Bank in Japan (DDBJ) Data Libraries under accession nos. AB554196–AB554222. The first 5 sequences and subsequent 20 sequences correspond to AFLP fragments and 20 BAC end sequences, respectively. Putative coding sequences of GmGIa, originating from Moshidou Gong 503, and GmGIb, originating from the Misuzudaizu allele, have been deposited under accession nos. AB554221 and AB554222, respectively. Sequences of the five BAC clones have been deposited under accession nos. AP011822 (WBb35C13), AP011811 (MiB300H01), AP011821 (WBb225N14), AP011813 (MiB319A04), and AP011810 (MiB039C03), respectively.

                [ 1 ] Corresponding author: Soybean Genome Research Team, National Institute of Agrobiological Sciences, 2-1-2 Kannondai, Tsukuba, Ibaraki 305-8602, Japan.   E-mail: haradaq@ 123456nias.affrc.go.jp
                Article
                125062
                10.1534/genetics.110.125062
                3122305
                21406680
                25fad4ff-e08c-48ba-9fe4-c3392033345f
                Copyright © 2011 by the Genetics Society of America

                Available freely online through the author-supported open access option.

                History
                : 10 November 2010
                : 3 March 2011
                Categories
                Investigations
                Genetics of Complex Traits

                Genetics
                Genetics

                Comments

                Comment on this article