Theoretical and Applied Genetics

, Volume 112, Issue 6, pp 1086–1097

Cloning and comparative analysis of the gene encoding diacylglycerol acyltransferase from wild type and cultivated soybean

Original Paper

DOI: 10.1007/s00122-006-0210-9

Cite this article as:
Wang, HW., Zhang, JS., Gai, JY. et al. Theor Appl Genet (2006) 112: 1086. doi:10.1007/s00122-006-0210-9
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Abstract

Diacylglycerol acyltransferase (DGAT), as an important enzyme in triacylglycerol synthesis, catalyzes the final acylation of the Kennedy pathway. In the present study, the GmDGAT gene was cloned from Glycine max by using AtDGAT as a query to search against the soybean EST database and the rapid amplification of cDNA ends (RACE) method. Allelic genes were also isolated from 13 soybean accessions and the divergence of the deduced amino acid sequences were compared. The comparison reveals that although GmDGAT is a highly conserved protein, several differences of insertion/deletion were identified in the N-terminal region of the GmDGATs from various soybean accessions. In the C-terminal regions, a single amino acid mutation specific to both G. max and G. soja was also found. The GmDGAT genomic sequences were further cloned and the number and size of exons in the DGAT genomic sequence were very similar among different plant species, whereas the introns were more diverged. These results may have significance in elucidating the genetic diversity of the GmDGAT among the soybean subgenus.

Keywords

Diacylglycerol acyltransferase gene Glycine max Diversity 

Copyright information

© Springer-Verlag 2006

Authors and Affiliations

  1. 1.The National Key Laboratory of Plant Genomics, Institute of Genetics and Developmental BiologyChinese Academy of SciencesBeijingChina
  2. 2.Graduate School of the Chinese Academy of SciencesBeijingChina
  3. 3.National soybean Institute for ImprovementNanjing UniversityNanjingChina

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