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Failure to maintain full-term pregnancies in pig carrying klotho monoallelic knockout fetuses

DC Field Value Language
dc.contributor.authorLee, Sanghoon-
dc.contributor.authorJung, Min Hee-
dc.contributor.authorSong, Kilyoung-
dc.contributor.authorJin, Jun-Xue-
dc.contributor.authorTaweechaipaisankul, Anukul-
dc.contributor.authorKim, Geon A-
dc.contributor.authorOh, Hyun Ju-
dc.contributor.authorKoo, Ok Jae-
dc.contributor.authorPark, Se Chang-
dc.contributor.authorLee, Byeong Chul-
dc.creator박세창-
dc.date.accessioned2021-02-22T07:26:27Z-
dc.date.available2021-02-22T16:28:54Z-
dc.date.issued2021-01-07-
dc.identifier.citationBMC Biotechnology. 2021 Jan 07;21(1):1ko_KR
dc.identifier.issn1472-6750-
dc.identifier.urihttps://hdl.handle.net/10371/173373-
dc.description.abstractBackground
Small animals that show a deficiency in klotho exhibit extremely shortened life span with multiple aging-like phenotypes. However, limited information is available on the function of klotho in large animals such as pigs.

Results
In an attempt to produce klotho knockout pigs, an sgRNA specific for klotho (targeting exon 3) was designed and Cas9-sgRNA ribonucleoproteins were transfected into porcine fibroblasts. Transfected fibroblasts were cultured for one to 2 days and then directly used for nuclear transfer without selection. The cloned embryos were cultured in vitro for 7 days and analyzed to detect modifications of the klotho gene by both T7E1 and deep sequencing analysis. Modification succeeded in 13 of 20 blastocysts (65%), 8 of which (40.0%) were monoallelic modifications and 5 (25.0%) were biallelic modifications. Based on high mutation rates in blastocysts, we transferred the cloned embryos to 5 recipient pigs; 1 recipient was pregnant and 16 fetuses were recovered at Day 28 post transfer. Of the 16 fetuses, 9 were resorbing and 7 were viable. Four of 9 (44.4%) resorbing fetuses and 3 of the 7 (42.9%) viable fetuses had monoallelic modifications. Thus, 3 klotho monoallelic knockout cell lines were established by primary culture. A total of 2088 cloned embryos reconstructed with 2 frame-shifted cell lines were transferred to 11 synchronized recipients. Of the recipients, 7 of 11 eleven (63.6%) became pregnant. However, none of the pregnancies was maintained to term. To discover why klotho monoallelic knockout fetuses were aborted, expression of aging- and apoptosis-related genes and klotho protein in placentas from klotho monoallelic knockout and wild-type fetuses was investigated. Placentas from klotho monoallelic knockout fetuses showed negatively changed expression of aging- and apoptosis-related genes with lower relative expression of klotho protein. These results indicated that the reason why klotho monoallelic knockout fetuses were not maintained to term was possibly due to decreased klotho expression in placentas, negatively affecting aging- and apoptosis-related genes.

Conclusions
Klotho monoallelic knockout porcine fetal fibroblasts were successfully established. However, pigs carrying klotho monoallelic knockout fetuses failed to maintain full-term pregnancy and a decrease in klotho expression in placenta likely leads to pregnancy loss.
ko_KR
dc.description.sponsorshipThis study was supported by the Korea Institute of Planning and Evaluation for Technology in Food, Agriculture, Forestry and Fisheries (#114059–03-3-SB010), the National Research Foundation (#2018R1D1A1B07048765), the Research Institute for Veterinary Science and the BK21 PLUS Program. The funding body had no role in the design of study, data collection, analysis
and interpretation, or writing of the manuscript.
ko_KR
dc.language.isoenko_KR
dc.publisherBMCko_KR
dc.subjectCRISPR/Cas9-
dc.subjectSomatic cell nuclear transfer-
dc.subjectKlotho-
dc.subjectAging-
dc.subjectPregnancy loss-
dc.titleFailure to maintain full-term pregnancies in pig carrying klotho monoallelic knockout fetusesko_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor이상훈-
dc.contributor.AlternativeAuthor정민희-
dc.contributor.AlternativeAuthor송길영-
dc.contributor.AlternativeAuthor김건아-
dc.contributor.AlternativeAuthor오현주-
dc.contributor.AlternativeAuthor구옥재-
dc.contributor.AlternativeAuthor박세창-
dc.contributor.AlternativeAuthor이병철-
dc.identifier.doi10.1186/s12896-020-00660-9-
dc.citation.journaltitleBMC Biotechnologyko_KR
dc.language.rfc3066en-
dc.rights.holderThe Author(s)-
dc.date.updated2021-01-27T09:24:13Z-
dc.citation.number1ko_KR
dc.citation.startpage1ko_KR
dc.citation.volume21ko_KR
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