Literature DB >> 18606825

Developmental disparity between in vitro-produced and somatic cell nuclear transfer bovine days 14 and 21 embryos: implications for embryonic loss.

Natalie I Alexopoulos1, Poul Maddox-Hyttel, Pernille Tveden-Nyborg, Nancy T D'Cruz, Tayfur R Tecirlioglu, Melissa A Cooney, Kirsten Schauser, Michael K Holland, Andrew J French.   

Abstract

In ruminants, the greatest period of embryonic loss coincides with the period of elongation when the embryonic disc is formed and gastrulation occurs prior to implantation. The impact of early embryonic mortality is not only a major obstacle to the cattle breeding industry but also impedes the application of new reproductive technologies such as somatic cell nuclear transfer (SCNT). In the present study, days 14 and 21 bovine embryos, generated by either in vitro-production (IVP) or SCNT, performed by either subzonal injection (SUZI) or handmade cloning (HMC), were compared by stereomicroscopy, immunohistochemistry, and transmission electron microscopy to establish in vivo developmental milestones. Following morphological examination, samples were characterized for the presence of epiblast (POU5F1), mesoderm (VIM), and neuroectoderm (TUBB3). On D14, only 25, 15, and 7% of IVP, SUZI, and HMC embryos were recovered from the embryos transferred respectively, and similar low recovery rates were noted on D21, suggesting that most of the embryonic loss had already occurred by D14. A number of D14 IVP, SUZI, and HMC embryos lacked an epiblast, but presented trophectoderm and hypoblast. When the epiblast was present, POU5F1 staining was limited to this compartment in all types of embryos. At the ultrastructural level, SCNT embryos displayed abundant secondary lysosomes and vacuoles, had fewer mitochondria, polyribosomes, tight junctions, desmosomes, and tonofilaments than their IVP counterparts. The staining of VIM and TUBB3 was less distinct in SCNT embryos when compared with IVP embryos, indicating slower or compromised development. In conclusion, SCNT and to some degree, IVP embryos displayed a high rate of embryonic mortality before D14 and surviving embryos displayed reduced quality with respect to ultrastructural features and differentiation markers.

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Year:  2008        PMID: 18606825     DOI: 10.1530/REP-07-0392

Source DB:  PubMed          Journal:  Reproduction        ISSN: 1470-1626            Impact factor:   3.906


  6 in total

Review 1.  BOARD INVITED REVIEW: Post-transfer consequences of in vitro-produced embryos in cattle.

Authors:  Alan D Ealy; Lydia K Wooldridge; Sarah R McCoski
Journal:  J Anim Sci       Date:  2019-05-30       Impact factor: 3.159

2.  Loss of methylation at H19 DMD is associated with biallelic expression and reduced development in cattle derived by somatic cell nuclear transfer.

Authors:  J Suzuki; J Therrien; F Filion; R Lefebvre; A K Goff; F Perecin; F V Meirelles; L C Smith
Journal:  Biol Reprod       Date:  2011-01-19       Impact factor: 4.285

Review 3.  Ruminant conceptus-maternal interactions: interferon-tau and beyond.

Authors:  Daniel J Mathew; Katie D Peterson; L Kirsten Senn; Mary A Oliver; Alan D Ealy
Journal:  J Anim Sci       Date:  2022-07-01       Impact factor: 3.338

4.  Uncoupled embryonic and extra-embryonic tissues compromise blastocyst development after somatic cell nuclear transfer.

Authors:  Séverine A Degrelle; Florence Jaffrezic; Evelyne Campion; Kim-Anh Lê Cao; Daniel Le Bourhis; Christophe Richard; Nathalie Rodde; Renaud Fleurot; Robin E Everts; Jérôme Lecardonnel; Yvan Heyman; Xavier Vignon; Xiangzhong Yang; Xiuchun C Tian; Harris A Lewin; Jean-Paul Renard; Isabelle Hue
Journal:  PLoS One       Date:  2012-06-06       Impact factor: 3.240

Review 5.  Genomic imprinting effects on complex traits in domesticated animal species.

Authors:  Alan M O'Doherty; David E MacHugh; Charles Spillane; David A Magee
Journal:  Front Genet       Date:  2015-04-24       Impact factor: 4.599

6.  DNA methylation dynamics at imprinted genes during bovine pre-implantation embryo development.

Authors:  Alan M O'Doherty; David A Magee; Lynee C O'Shea; Niamh Forde; Marijke E Beltman; Solomon Mamo; Trudee Fair
Journal:  BMC Dev Biol       Date:  2015-03-10       Impact factor: 1.978

  6 in total

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