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Placental imprinting of SLC22A3 in the IGF2R imprinted domain is conserved in therian mammals

BACKGROUND: The eutherian IGF2R imprinted domain is regulated by an antisense long non-coding RNA, Airn, which is expressed from a differentially methylated region (DMR) in mice. Airn silences two neighbouring genes, Solute carrier family 22 member 2 (Slc22a2) and Slc22a3, to establish the Igf2r imp...

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Autores principales: Ishihara, Teruhito, Griffith, Oliver W., Suzuki, Shunsuke, Renfree, Marilyn B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9419357/
https://www.ncbi.nlm.nih.gov/pubmed/36030241
http://dx.doi.org/10.1186/s13072-022-00465-4
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author Ishihara, Teruhito
Griffith, Oliver W.
Suzuki, Shunsuke
Renfree, Marilyn B.
author_facet Ishihara, Teruhito
Griffith, Oliver W.
Suzuki, Shunsuke
Renfree, Marilyn B.
author_sort Ishihara, Teruhito
collection PubMed
description BACKGROUND: The eutherian IGF2R imprinted domain is regulated by an antisense long non-coding RNA, Airn, which is expressed from a differentially methylated region (DMR) in mice. Airn silences two neighbouring genes, Solute carrier family 22 member 2 (Slc22a2) and Slc22a3, to establish the Igf2r imprinted domain in the mouse placenta. Marsupials also have an antisense non-coding RNA, ALID, expressed from a DMR, although the exact function of ALID is currently unknown. The eutherian IGF2R DMR is located in intron 2, while the marsupial IGF2R DMR is located in intron 12, but it is not yet known whether the adjacent genes SLC22A2 and/or SLC22A3 are also imprinted in the marsupial lineage. In this study, the imprinting status of marsupial SLC22A2 and SLC22A3 in the IGF2R imprinted domain in the chorio-vitelline placenta was examined in a marsupial, the tammar wallaby. RESULTS: In the tammar placenta, SLC22A3 but not SLC22A2 was imprinted. Tammar SLC22A3 imprinting was evident in placental tissues but not in the other tissues examined in this study. A putative promoter of SLC22A3 lacked DNA methylation, suggesting that this gene is not directly silenced by a DMR on its promoter as seen in the mouse. Based on immunofluorescence, we confirmed that the tammar SLC22A3 is localised in the endodermal cell layer of the tammar placenta where nutrient trafficking occurs. CONCLUSIONS: Since SLC22A3 is imprinted in the tammar placenta, we conclude that this placental imprinting of SLC22A3 has been positively selected after the marsupial and eutherian split because of the differences in the DMR location. Since SLC22A3 is known to act as a transporter molecule for nutrient transfer in the eutherian placenta, we suggest it was strongly selected to control the balance between supply and demand of nutrients in marsupial as it does in eutherian placentas. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13072-022-00465-4.
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spelling pubmed-94193572022-08-28 Placental imprinting of SLC22A3 in the IGF2R imprinted domain is conserved in therian mammals Ishihara, Teruhito Griffith, Oliver W. Suzuki, Shunsuke Renfree, Marilyn B. Epigenetics Chromatin Research BACKGROUND: The eutherian IGF2R imprinted domain is regulated by an antisense long non-coding RNA, Airn, which is expressed from a differentially methylated region (DMR) in mice. Airn silences two neighbouring genes, Solute carrier family 22 member 2 (Slc22a2) and Slc22a3, to establish the Igf2r imprinted domain in the mouse placenta. Marsupials also have an antisense non-coding RNA, ALID, expressed from a DMR, although the exact function of ALID is currently unknown. The eutherian IGF2R DMR is located in intron 2, while the marsupial IGF2R DMR is located in intron 12, but it is not yet known whether the adjacent genes SLC22A2 and/or SLC22A3 are also imprinted in the marsupial lineage. In this study, the imprinting status of marsupial SLC22A2 and SLC22A3 in the IGF2R imprinted domain in the chorio-vitelline placenta was examined in a marsupial, the tammar wallaby. RESULTS: In the tammar placenta, SLC22A3 but not SLC22A2 was imprinted. Tammar SLC22A3 imprinting was evident in placental tissues but not in the other tissues examined in this study. A putative promoter of SLC22A3 lacked DNA methylation, suggesting that this gene is not directly silenced by a DMR on its promoter as seen in the mouse. Based on immunofluorescence, we confirmed that the tammar SLC22A3 is localised in the endodermal cell layer of the tammar placenta where nutrient trafficking occurs. CONCLUSIONS: Since SLC22A3 is imprinted in the tammar placenta, we conclude that this placental imprinting of SLC22A3 has been positively selected after the marsupial and eutherian split because of the differences in the DMR location. Since SLC22A3 is known to act as a transporter molecule for nutrient transfer in the eutherian placenta, we suggest it was strongly selected to control the balance between supply and demand of nutrients in marsupial as it does in eutherian placentas. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13072-022-00465-4. BioMed Central 2022-08-27 /pmc/articles/PMC9419357/ /pubmed/36030241 http://dx.doi.org/10.1186/s13072-022-00465-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Ishihara, Teruhito
Griffith, Oliver W.
Suzuki, Shunsuke
Renfree, Marilyn B.
Placental imprinting of SLC22A3 in the IGF2R imprinted domain is conserved in therian mammals
title Placental imprinting of SLC22A3 in the IGF2R imprinted domain is conserved in therian mammals
title_full Placental imprinting of SLC22A3 in the IGF2R imprinted domain is conserved in therian mammals
title_fullStr Placental imprinting of SLC22A3 in the IGF2R imprinted domain is conserved in therian mammals
title_full_unstemmed Placental imprinting of SLC22A3 in the IGF2R imprinted domain is conserved in therian mammals
title_short Placental imprinting of SLC22A3 in the IGF2R imprinted domain is conserved in therian mammals
title_sort placental imprinting of slc22a3 in the igf2r imprinted domain is conserved in therian mammals
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9419357/
https://www.ncbi.nlm.nih.gov/pubmed/36030241
http://dx.doi.org/10.1186/s13072-022-00465-4
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