Characterization of genes encoding Starch Branching Enzyme I from Triticum monococcum and its diploid wheat relatives

Biologia ◽  
2015 ◽  
Vol 70 (9) ◽  
pp. 1193-1200
Author(s):  
Xiu-Ying Wang ◽  
Chang-Shui Wang ◽  
Jian Ma ◽  
Ji-Rui Wang ◽  
Ya-Xi Liu ◽  
...  

Abstract The Starch Branching Enzyme I (SBEI) gene plays an important role in amylopectin synthesis. Here, we isolated and characterized the full-length cDNA and DNA sequences of SBEI gene from diploid Triticeae species, Triticum monococcum, T. urartu, Aegilopsspeltoides, and Ae. tauschii. Then we predicted its protein structure, analyzed its evolutionary relationship with other species, and explored its expression patterns using real-time quantitative PCR. The SBEI cDNA includes a 2,490-bp open reading frame (ORF) encoding 829 amino acids. The genomic DNA of SBEI is 5,526-bp in length, containes fourteen exons and thirteen introns, and shares a similar structure with its homologous genes from other cereal plants. Sequence similarity ranging from 70.50% to 98.02% in exons and from 15.50% to 83.63% in introns was detected. Results of phylogenetic tree based on the deduced amino acid sequences from T. monococcum and other plants indicated that T. monococcum SBEI is more closely related to T. boeoticum and T. urartu. Expression analysis revealed that T. monococcum SBEI and AGPase genes were highly expressed in the seeds at middle developmental stage. This is the first report on characterization of the SBEI gene in T. monococcum. These results could be used to explore the roles of this enzyme in amylopectin synthesis.

2010 ◽  
Vol 58 (19) ◽  
pp. 10437-10444 ◽  
Author(s):  
Jia-Wei Chang ◽  
Sing-Chung Li ◽  
Yun-Chi Shih ◽  
Reuben Wang ◽  
Pei-Shan Chung ◽  
...  

1996 ◽  
Vol 30 (6) ◽  
pp. 1223-1232 ◽  
Author(s):  
Ming Gao ◽  
Dane K. Fisher ◽  
Kyung-Nam Kim ◽  
Jack C. Shannon ◽  
Mark J. Guiltinan

2015 ◽  
Vol 67 (7-8) ◽  
pp. 663-672 ◽  
Author(s):  
Xiu-Ying Wang ◽  
Jian Ma ◽  
Chang-Shui Wang ◽  
Ling-Ling Zhang ◽  
Ji-Rui Wang ◽  
...  

Genome ◽  
2008 ◽  
Vol 51 (11) ◽  
pp. 871-877 ◽  
Author(s):  
Marilena Ceccarelli ◽  
Vania Sarri ◽  
Stefania Minelli ◽  
Maria Teresa Gelati

DNA sequences belonging to two families of tandem repeats, PpeRsa1 (362–364 bp in length, 62% A+T residues) and PpeRsa2 (355–359 bp in length, 59% A+T residues), have been isolated from the Potamogeton pectinatus L. genome. The two sequence families do not share significant nucleotide sequence similarity, even if an evolutionary relationship between them could be assumed. The comparison of the cleaving activity of isoschizomeres that are either sensitive or insensitive to methylation of cytosine residues in the target sequence revealed high methylation in both sequence families. The copy number per 1C DNA of PpeRsa1- and PpeRsa2-related sequences is estimated to be 4.92 × 104 and 7.96 × 104, respectively. Taken together, these sequences account for about 7.5% of the entire genome of P. pectinatus. The chromosomal organization of these sequences was investigated by fluorescent in situ hybridization. PpeRsa1 and PpeRsa2 repeats found related sequences in 52 chromosomes of the P. pectinatus complement (2n = 78). The related sequences were localized around the centromeres and at the chromosome ends in three pairs of chromosomes, while they were found only at the chromosome ends in the remaining pairs. Twenty-six chromosomes did not show any hybridization signal. The hypothesis that the species is a hybrid between a diploid parent and an allotetraploid parent is put forward.


2008 ◽  
Vol 72 (11) ◽  
pp. 2858-2866 ◽  
Author(s):  
Nhuan Thi VU ◽  
Hiroaki SHIMADA ◽  
Yoshimitsu KAKUTA ◽  
Takashi NAKASHIMA ◽  
Hiroko IDA ◽  
...  

2018 ◽  
Vol 68 (2) ◽  
pp. 278-283 ◽  
Author(s):  
Takuya Wada ◽  
Osamu Yamaguchi ◽  
Masayuki Miyazaki ◽  
Katsunori Miyahara ◽  
Masafumi Ishibashi ◽  
...  

2001 ◽  
Vol 268 (23) ◽  
pp. 6140-6145 ◽  
Author(s):  
Ulrika Rydberg ◽  
Lena Andersson ◽  
Roger Andersson ◽  
Per Åman ◽  
Håkan Larsson

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