The invention relates to a
cloning and function expression method of an adversity stress AhMYBL6
gene in peanut. The adversity stress AhMYBL6
gene is synthesized by RT-PCR (reverse transcription-
polymerase chain reaction)
cloning by the steps of preparation and treatment of materials, extraction of
RNA (ribonucleic acid) and synthesis of cDNA (
complementary deoxyribonucleic acid). The
open reading frame of the
gene is 861bp, and 287 amino acids are coded totally. The homology of the
amino acid sequence of the gene with the
MYb family proteins GmMYB4, GmMYB29 and GmMYB29A2 of the soybean is higher than 60%. The fluorescent quantitative PCR verifies the expression patterns of the AhMYBL6 under low temperature, salt stress and
drought stress; the result indicates that the expression levels of the AhMYBL6 are obviously enhanced after various stress treatment for 1 hour, and kept at high levels all the time thereafter; and the expression level of the AhMYBL6 in the leaf subjected to low-
temperature treatment is maximally enhanced by 20 times. After the gene is transferred into peanut by transgenic means, compared with the control, the transgenic
plant has obvious characteristics of
cold tolerance, salt tolerance and
drought tolerance. The AhMYBL6 gene can obviously enhance the stress tolerance of the peanut.