Soybean regulatory elements and uses thereof
A technology of nucleotide sequences and expression cassettes, applied in the field of regulatory elements, can solve problems such as limited selection
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example 1
[0109] Example 1: Identification and Characterization of Novel Promoter Sequences
[0110] method
[0111] Using reference genomes from wild Soybean species (Glycine max, Glycine max, Penghu Soybean and Glycine max) and based on the analysis of certain genes from soybean: ubiquitin (Ubi), s-adenosylmethionine Identification of orthologs of (SAM), actin depolymerization factor (ADF3), and translation elongation factor EF-1α (EF1a) resulted in candidate promoter sequences. Additional candidate promoter sequences were identified using RNAseq data to identify genes in soybean expressed between 12-18 log2 normalized data, and putative promoter sequences from these genes were added as candidates. Candidate promoter sequences are 2 kb regions upstream of the predicted or known translation start site. Candidate promoter sequences are expected to contain basal promoter elements, as well as the 5'UTR and possibly introns (depending on the predicted or known structure of the coding s...
example 2
[0137] Taken together, these data show that the four selected candidate promoters are highly expressed in a variety of tissues and are expected to be useful as constitutive promoters for use in expression constructs in soybean. Example 2: Identification and Characterization of Novel Terminator Sequences
[0138] method
[0139] Candidate terminator sequences were derived from the genes tested in Example 1 and tested for terminator activity. Candidate terminator sequences are 1 kb regions downstream of predicted or known translation termination sites. Candidate terminator sequences are expected to contain the 3' UTR and possibly additional 3' non-transcribed sequences (depending on the predicted or known structure of the coding sequence).
[0140] Vectors were designed for each candidate terminator, each containing Bx9 as a reporter gene and the promoter sequence prGmSAMS (SEQ ID NO: 7). Vectors were first screened by transient transformation using the method described in ...
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