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Identification of a novel MLPK homologous gene MLPKn1 and its expression analysis in Brassica oleracea

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Abstract

M locus protein kinase, one of the SRK-interacting proteins, is a necessary positive regulator for the self-incompatibility response in Brassica. In B. rapa, MLPK is expressed as two different transcripts, MLPKf1 and MLPKf2, and either isoform can complement the mlpk/mlpk mutation. The AtAPK1B gene has been considered to be the ortholog of BrMLPK, and AtAPK1B has no role in self-incompatibility (SI) response in A. thaliana SRK–SCR plants. Until now, what causes the MLPK and APK1B function difference during SI response in Brassica and A. thaliana SRKb–SCRb plants has remained unknown. Here, in addition to the reported MLPKf1/2, we identified the new MLPKf1 homologous gene MLPKn1 from B. oleracea. BoMLPKn1 and BoMLPKf1 shared nucleotide sequence identity as high as 84.3 %, and the most striking difference consisted in two fragment insertions in BoMLPKn1. BoMLPKn1 and BoMLPKf1 had a similar gene structure; both their deduced amino acid sequences contained a typical plant myristoylation consensus sequence and a Ser/Thr protein kinase domain. BoMLPKn1 was widely expressed in petal, sepal, anther, stigma and leaf. Genome-wide survey revealed that the B. oleracea genome contained three MLPK homologous genes: BoMLPKf1/2, BoMLPKn1 and Bol008343n. The B. rapa genome also contained three MLPK homologous genes, BrMLPKf1/2, BraMLPKn1 and Bra040929. Phylogenetic analysis revealed that BoMLPKf1/2 and BrMLPKf1/2 were phylogenetically more distant from AtAPK1A than Bol008343n, Bra040929, BraMLPKn1 and BoMLPKn1, Synteny analysis revealed that the B. oleracea chromosomal region containing BoMLPKn1 displayed high synteny with the A. thaliana chromosomal region containing APK1B, whereas the B. rapa chromosomal region containing BraMLPKn1 showed high synteny with the A. thaliana chromosomal region containing APK1B. Together, these results revealed that BoMLPKn1/BraMLPKn1, and not the formerly reported BoMLPKf1/2 (BrMLPKf1/2), was the orthologous genes of AtAPK1B, and no ortholog of BoMLPKf1/2 (BrMLPKf1/2) was found in the A. thaliana genome. We speculated that Brassica MLPKf1/2 might have emerged after speciation of Brassica and A. thailiana, and that it was recruited to the SRK-triggered SI signaling cascade in Brassica.

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Acknowledgments

This work was supported by the Chongqing Natural Science Foundation (cstc2012jjB80010), the Fundamental Research Funds for the Central Universities (XDJK2010B010), the National Basic Research Program of China (‘973’ Program, 2012CB113900) and the Natural Science Foundation of China (30900986, 30971849, 31572127).

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    1. Key Laboratory of Horticulture Science for Southern Mountainous Regions, Ministry of Education/College of Horticulture and Landscape Architecture, Southwest University, Chongqing, 400715, China

      Qiguo Gao, Songmei Shi, Yudong Liu, Quanming Pu, Xiaohuan Liu & Ying Zhang

    2. College of Agronomy and Biotechnology, Southwest University, Chongqing, 400715, China

      Liquan Zhu

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    1. Qiguo Gao
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    Communicated by Dolf Weijers.

    Qiguo Gao, Songmei Shi and Yudong Liu have contributed equally to this work.

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    Gao, Q., Shi, S., Liu, Y. et al. Identification of a novel MLPK homologous gene MLPKn1 and its expression analysis in Brassica oleracea . Plant Reprod 29, 239–250 (2016). https://doi.org/10.1007/s00497-016-0287-5

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