Abstract:The cDNA and genomic clones from sweet potato encoding granule-bound starch synthase I (GBSSI) were isolated and characterized. The sequence analysis of the cDNA shows that the sweet potato GBSSI mature protein is comprised of 531 amino acids and that the precursor has a transit peptide of 77 amino acids.
“…The peptide was similar in size to the GBSSI transit peptide of sweet potato (Kimura et al 2000), potato (van der Leij et al 1991), and cassava (Salehuzzaman et al 1993). The transit peptide of amaranth has 43.7% identity over amino acids with that of the sweet potato but much less with other plant species (14.1~32.9%) ( Table 4).…”
Section: Transit Peptide Predictionmentioning
confidence: 85%
“…3). This structure is similar to that of the nonwaxy type characterized in other species such as maize (Klosgen et al Table 3. 1986), rice (Okagaki 1992), foxtail millet (Fukunaga et al 2002), potato (van der Leij et al 1991, and sweet potato (Kimura et al 2000). All five-plant species contain 14 exons, with exons 2-14 (13 exons) contributing to the coding sequence.…”
Section: Isolation and Characterization Of The Gbssi Gene In Amaranthmentioning
confidence: 99%
“…To date, sequence information of the GBSSI structural genes from several species, such as maize (Klosgen et al 1986), rice (Okagaki 1992), barley (Rohde et al 1988), wheat (Clark et al 1991, Murai et al 1999, potato (van der Leij et al 1991), sweet potato (Kimura et al 2000) and foxtail millet (Fukunaga et al 2002) have been published. To facilitate further studies of amaranth starch, it is essential to characterize the GBSSI gene and to establish its primary structures.…”
A full-length cDNA clone encoding granule-bound starch synthase I (GBSSI = Waxy gene) from grain amaranth (Amaranthus cruentus L.) perisperm was isolated and characterized. Segregation of amylose content in F 2 population suggested that the amylose content of A cruentus is controlled by a single gene, Waxy (GBSSI). cDNA clone of this gene is 2076 bp in length and contains an open reading frame of 1821 bp corresponding to a polypeptide of 606 amino acids residues, including a transit peptide of 77 amino acids. Comparison of the cDNA and genomic sequences (3492 bp) suggested that the amaranth GBSSI gene has 12 introns, of which exons 1-13 contributed to the coding sequence. The mature protein shares 70.2-75.3% sequence identity with GBSSI of dicots and about 64.0-67.8% identity with those of monocots. This protein contains the conserved motif KTGGL found in other GBSSI proteins, which has been implicated as the active site in glycogen synthase. Sequence analysis predicted that GBSSI of amaranth has a transit peptide of 77 amino acids including FIR↓S, which is different cleavage site that of the other dicot species. These results will provide more useful information for understanding the structure/function relationship of this protein from amaranths perisperm.
“…The peptide was similar in size to the GBSSI transit peptide of sweet potato (Kimura et al 2000), potato (van der Leij et al 1991), and cassava (Salehuzzaman et al 1993). The transit peptide of amaranth has 43.7% identity over amino acids with that of the sweet potato but much less with other plant species (14.1~32.9%) ( Table 4).…”
Section: Transit Peptide Predictionmentioning
confidence: 85%
“…3). This structure is similar to that of the nonwaxy type characterized in other species such as maize (Klosgen et al Table 3. 1986), rice (Okagaki 1992), foxtail millet (Fukunaga et al 2002), potato (van der Leij et al 1991, and sweet potato (Kimura et al 2000). All five-plant species contain 14 exons, with exons 2-14 (13 exons) contributing to the coding sequence.…”
Section: Isolation and Characterization Of The Gbssi Gene In Amaranthmentioning
confidence: 99%
“…To date, sequence information of the GBSSI structural genes from several species, such as maize (Klosgen et al 1986), rice (Okagaki 1992), barley (Rohde et al 1988), wheat (Clark et al 1991, Murai et al 1999, potato (van der Leij et al 1991), sweet potato (Kimura et al 2000) and foxtail millet (Fukunaga et al 2002) have been published. To facilitate further studies of amaranth starch, it is essential to characterize the GBSSI gene and to establish its primary structures.…”
A full-length cDNA clone encoding granule-bound starch synthase I (GBSSI = Waxy gene) from grain amaranth (Amaranthus cruentus L.) perisperm was isolated and characterized. Segregation of amylose content in F 2 population suggested that the amylose content of A cruentus is controlled by a single gene, Waxy (GBSSI). cDNA clone of this gene is 2076 bp in length and contains an open reading frame of 1821 bp corresponding to a polypeptide of 606 amino acids residues, including a transit peptide of 77 amino acids. Comparison of the cDNA and genomic sequences (3492 bp) suggested that the amaranth GBSSI gene has 12 introns, of which exons 1-13 contributed to the coding sequence. The mature protein shares 70.2-75.3% sequence identity with GBSSI of dicots and about 64.0-67.8% identity with those of monocots. This protein contains the conserved motif KTGGL found in other GBSSI proteins, which has been implicated as the active site in glycogen synthase. Sequence analysis predicted that GBSSI of amaranth has a transit peptide of 77 amino acids including FIR↓S, which is different cleavage site that of the other dicot species. These results will provide more useful information for understanding the structure/function relationship of this protein from amaranths perisperm.
“…To date, the waxy structural genes have been characterized from wheat (Murai et al, 1999), maize (Klösgeni et al, 1986), rice (Wang et al, 1990;Okagaki, 1992), barley (Rohde et al, 1988), rye (Mason-Gamer, 2001;Xu et al, 2009), sorghum (Hsieh et al, 1996), potato (van der Leij et al, 1991), pea (Dry et al, 1992), cassava (Salehuzzaman et al, 1993) potato (Kimura et al, 2000), foxtail millet (Fukunaga et al, 2002) and amaranth (Park et al, 2009a). The loss of GBSS function in cereal crops can produce the waxy phenotype which is featured by the altered texture and appearance of starchy endosperms (Denyer et al, 2001).…”
Two alleles of the barley waxy locus were characterized from non-waxy cultivar Bowman and waxy cultivar CDC Candle, respectively. Their nucleotide and protein sequences were compared with other known waxy genes. The comparison results indicated that there were 100 polymorphic sites, among which 69 were in the non-coding region and 31 were in the coding region. Out of 100 polymorphic sites, 45 were transversion, 35 were transition and 20 were indels. A 397 bp deletion and a 193 bp insertion in the promoter region and a 15 bp insertion in the coding region were found in CDC Candle, but not in Bowman. A deletion (11 bp) was detected in Bowman, which exhibited no effects on normal waxy expression. In summary, the 397 bp deletion was supposed to account for the reduction of GBSS I, resulting in the low amylose in CDC Candle; whereas other polymorphic sites might be not correlated with amylose synthesis.
“…Since low or no amylose production leads to waxy endosperm, the GBSSI gene is also known as waxy gene. Because of the importance of GBSSI gene to influence starch quality, it has been characterized and studied in many crop plants, including cereal grain plants of the family Poaceae, such as rice (Sano, 1984), maize (Tsai, 1974), barley (Patron et al, 2002), bread and durum wheat (Fujita et al, 2001;Lafiandra et al, 2010;Miura et al, 1994;Nakamura et al, 1995) and foxtail millet (Fukunaga et al, 2002), tuber plants, such as potato (van der Leij et al, 1991), sweet potato (Kimura et al, 2000) and cassava (Salehuzzaman et al, 1993), and some important food crops and herb crops, e.g. peas (Edwards, 2002).…”
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