Evolutionary origins of the placental expression of chromosome 19 cluster galectins and their complex dysregulation in preeclampsia

N. G. Than, R. Romero, Y. Xu, O. Erez, Z. Xu, G. Bhatti, R. Leavitt, T. H. Chung, H. El-Azzamy, C. Lajeunesse, B. Wang, A. Balogh, G. Szalai, S. Land, Z. Dong, S. S. Hassan, T. Chaiworapongsa, M. Krispin, C. J. Kim, A. L. TarcaZ. Papp, H. Bohn

    Research output: Contribution to journalArticlepeer-review

    71 Scopus citations


    Introduction: The dysregulation of maternal-fetal immune tolerance is one of the proposed mechanisms leading to preeclampsia. Galectins are key regulator proteins of the immune response in vertebrates and maternal-fetal immune tolerance in eutherian mammals. Previously we found that three genes in a Chr19 cluster encoding for human placental galectin-13 (PP13), galectin-14 and galectin-16 emerged during primate evolution and may confer immune tolerance to the semi-allogeneic fetus. Materials and Methods: This study involved various methodologies for gene and protein expression profiling, genomic DNA methylation analyses, functional assays on differentiating trophoblasts including gene silencing, luciferase reporter and methylation assays. These methods were applied on placental specimens, umbilical cord blood cells, primary trophoblasts and BeWo cells. Genomic DNA sequences were analyzed for transposable elements, transcription factor binding sites and evolutionary conservation. Results and Discussion: The villous trophoblastic expression of Chr19 cluster galectin genes is developmentally regulated by DNA methylation and induced by key transcription factors of villous placental development during trophoblast fusion and differentiation. This latter mechanism arose via the co-option of binding sites for these transcription factors through promoter evolution and the insertion of an anthropoid-specific L1PREC2 transposable element into the 5 untranslated region of an ancestral gene followed by gene duplication events. Among placental Chr19 cluster galectin genes, the expression of LGALS13 and LGALS14 is down-regulated in preterm severe preeclampsia associated with SGA. We reveal that this phenomenon is partly originated from the dysregulated expression of key transcription factors controlling trophoblastic functions and galectin gene expression. In addition, the differential DNA methylation of these genes was also observed in preterm preeclampsia irrespective of SGA. Conclusions: These findings reveal the evolutionary origins of the placental expression of Chr19 cluster galectins. The complex dysregulation of these genes in preeclampsia may alter immune tolerance mechanisms at the maternal-fetal interface.

    Original languageEnglish
    Pages (from-to)855-865
    Number of pages11
    Issue number11
    StatePublished - 1 Nov 2014


    • ALU AP2
    • Anthropoid primate
    • ESRRG
    • Epigenome
    • GATA
    • GCM1
    • LINE
    • Lectin
    • PP13 Pregnancy Syncytiotrophoblast TEF5

    ASJC Scopus subject areas

    • Reproductive Medicine
    • Obstetrics and Gynecology
    • Developmental Biology


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