MicroRNAs, polyamines, and the activities antioxidant enzymes are associated with in vitro rooting in white pine (Pinus strobus L.)

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Abstract

Molecular mechanism of in vitro rooting in conifer is not fully understood. After establishment of a regeneration procedure in eastern white pine (Pinus strobus L.) using mature embryos as explants to induce shoot formation on medium containing 3 μM IAA, 6 μM BA and 6 μM TDZ and induce root formation on medium containing 0.001-0.05 μM IAA, 0.001–0.05 μM IBA, 0.001–0.05 μM TDZ, we have investigated the changes of polyamine content and the activities of antioxidant enzymes during in vitro rooting in P. strobus. Our results demonstrated that putrescine (Put), spermidine (Spd), and spermine (Spm) did not increase in P. strobus during the first week of rooting on medium supplemented with 0.01 μM indole-3-acetic acid (IAA), whereas the levels of Put, Spd, and Spm increased during the 1st–3rd week of culture on medium with IAA, and then decreased on medium with IAA. No such a change in Put, Spd, and Spm was observed on medium without IAA. Measurement of antioxidant enzyme activity demonstrated that the activities of polyphenol oxidase, catalase, and peroxidase slightly increased in the first week of culture and reached to the highest peak in the 3rd–5th week of culture. Quantitative RT-PCR results indicated that miR160 was increased on the 7th day, miR162, miR397, and miR408 was increased from the 21th to 35th day, miR857 was increased on the 35th day, and miR827 was increased on the 49th day. These results demonstrated that enhanced polyamine biosynthesis, antioxidant enzyme activity, and microRNAs are correlated with the root induction and formation in P. strobus.

Figures

  • Fig. 1 In vitro rooting of P. strobus. a Root formation from elongated adventitious shoots at different time points of culture on media with 0.01 μM IAA. Roots formed from elongated adventitious shoots were shown at 7, 21, 35, and 49 days of culture. b Rooting rate of shoots derived from genotypes 1-721, 2-007, 3-011, and 3-101 on medium containing 0.01 μM IAA. Each treatment was replicated five times, and each replicate consisted of 30–50 shoots. Values represent the mean ± SD. Values followed by one asterisk are significantly different from the corresponding control value (P < 0.05; n = 5) by ANOVA
  • Table 1 Effect of IAA on the percentage of rooting shoots in P. strobus
  • Table 2 Effect of IBA on the percentage of rooting shoots in P. strobus
  • Table 3 Effect of TDZ on the percentage of rooting shoots in P. strobus
  • Fig. 2 Changes of polyamines a putrescine (Put), b spermidine (Spd), and c spermine (Spm) levels during rooting. Polyamines contents were measured 7, 21, 35, and 49 days after shoots were transferred into media containing 0.01 μM IAA. Shoots for the control were derived from genotype 1-721 and were transferred to media without IAA. Each experiment was replicated five times, and each replicate consisted of 6–8 samples. Values represent the mean ± SD. Values followed by one asterisk are significantly different from the corresponding control value (P < 0.05; n = 5) by ANOVA
  • Fig. 3 Changes of antioxidant enzyme activity during rooting. Activities of a PPO, b CAT, and c POD were measured 7, 21, 35, and 49 days after shoots were transferred into media containing 0.01 μM IAA. Shoots for the control were derived from genotype 1-721 and were transferred to media without IAA. Each experiment was replicated five times, and each replicate consisted of 6–8 samples. Values represent the mean ± SD. Values followed by one asterisk are significantly different from the corresponding control value (P < 0.05; n = 5) by ANOVA
  • Fig. 4 Expression of miRNAs during the time course of in vitro rooting in P. strobus. RNA was isolated from seedlings at different stages (7, 21, 35, 49 days) of rooting after shoots were transferred into media containing 0.01 μM IAA. Shoots for the control were derived from genotype 1-721 and were transferred to media without IAA. Relative expression was indicated by the log2 value. Values followed by one asterisk are significantly different from the corresponding control value (P < 0.05; n = 3) by ANOVA
  • Table 4 Primers used for  amplification of  microRNA expression

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APA

Fei, Y., Xiao, B., Yang, M., Ding, Q., & Tang, W. (2016). MicroRNAs, polyamines, and the activities antioxidant enzymes are associated with in vitro rooting in white pine (Pinus strobus L.). SpringerPlus, 5(1). https://doi.org/10.1186/s40064-016-2080-1

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