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Title: Expression of human mutant cyclin dependent kinase 4, Cyclin D and telomerase extends the life span but does not immortalize fibroblasts derived from loggerhead sea turtle (Caretta caretta)
Authors: Fukuda, Tomokazu
Eitsuka, Takahiro
Donai, Kenichiro
Kurita, Masanori
Saito, Tomomi
Okamoto, Hitoshi
Kinoshita, Kodzue  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0002-5804-5485 (unconfirmed)
Katayama, Masafumi
Nitto, Hiroshi
Uchida, Takafumi
Onuma, Manabu
Sone, Hideko
Inoue-Murayama, Miho
Kiyono, Tohru
Author's alias: 木下, こづえ
Issue Date: Dec-2018
Publisher: Springer Nature
Journal title: Scientific reports
Volume: 8
Start page: 9229
End page: 9229
Abstract: Conservation of the genetic resources of endangered animals is crucial for future generations. The loggerhead sea turtle (Caretta caretta) is a critically endangered species, because of human hunting, hybridisation with other sea turtle species, and infectious diseases. In the present study, we established primary fibroblast cell lines from the loggerhead sea turtle, and showed its species specific chromosome number is 2n = 56, which is identical to that of the hawksbill and olive ridley sea turtles. We first showed that intensive hybridization among multiple sea turtle species caused due to the identical chromosome number, which allows existence of stable hybridization among the multiple sea turtle species. Expressions of human-derived mutant Cyclin-dependent kinase 4 (CDK4) and Cyclin D dramatically extended the cell culture period, when it was compared with the cell culture period of wild type cells. The recombinant fibroblast cell lines maintained the normal chromosome condition and morphology, indicating that, at the G1/S phase, the machinery to control the cellular proliferation is evolutionally conserved among various vertebrates. To our knowledge, this study is the first to demonstrate the functional conservation to overcome the negative feedback system to limit the turn over of the cell cycle between mammalian and reptiles. Our cell culture method will enable the sharing of cells from critically endangered animals as research materials.
Rights: © The Author(s) 2018 This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
URI: http://hdl.handle.net/2433/261877
DOI(Published Version): 10.1038/s41598-018-27271-x
PubMed ID: 29925962
Appears in Collections:Journal Articles

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