Vascular alterations underlie developmental problems manifested in cloned cattle before or after birth

Although assisted reproductive techniques are commonly applied in humans and animals, they are frequently associated with major developmental deficits and reduced viability. To explore abnormalities associated with cloning or nuclear transfer (NT) as the most invasive of these methods, we used a bov...

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Published in:PloS one Vol. 10; no. 1; p. e0106663
Main Authors: Maiorka, Paulo Cesar, Favaron, Phelipe Oliveira, Mess, Andrea Maria, dos Santos, Caio Rodrigues, Alberto, Miryan Lanca, Meirelles, Flavio Vieira, Miglino, Maria Angelica
Format: Journal Article
Language:English
Published: United States Public Library of Science 13-01-2015
Public Library of Science (PLoS)
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Summary:Although assisted reproductive techniques are commonly applied in humans and animals, they are frequently associated with major developmental deficits and reduced viability. To explore abnormalities associated with cloning or nuclear transfer (NT) as the most invasive of these methods, we used a bovine model to characterize abnormalities. Detailed necropsy examinations were done on 13 calves that died soon after birth; in addition, we included data from embryos and fetuses (produced by NT) that terminated prematurely. Bovine clones that survived until the neonatal period differed quantitatively and qualitatively from in-vivo-derived cattle. Although alterations affected a variety of organs (e.g. heart, lung and liver), there was a clear association with abberant vascular developmental during the early intrauterine phase. Therefore, we concluded that vascular problems were key alterations induced by cloning (presumably via epigenetic modifications).
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Competing Interests: The authors have declared that no competing interests exist.
Conceived and designed the experiments: PCM FVM MAM. Performed the experiments: MLA FVM. Analyzed the data: PCM CRS POF AMM. Contributed reagents/materials/analysis tools: FVM MAM. Wrote the paper: PCM POF AMM MAM.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0106663