Architectural defects in pronuclei of mouse nuclear transplant embryos

Reprogramming somatic nuclear function by transplantation of nuclei into recipient oocytes is associated with a morphological remodeling of the somatic nucleus. Successful cloning of animals by nuclear transplantation (NT) demonstrates that reprogramming somatic cell function is possible. However, low pregnancy rates and high frequencies of lethal abnormalities in animals born suggest that reprogramming is rarely complete. To address this issue, we tested the hypothesis that nuclear transplantation leads to nuclear remodeling deficiencies. We report the identification of several markers of morphological remodeling, or lack thereof, of mouse cumulus cell nuclei after transplantation into oocytes. Notably, nuclear transplant mouse embryos exhibit nuclear assembly of the differentiated cell-specific A-type lamins at the one-cell stage, as a result of misregulation of lamin A gene expression. The transplanted nuclei also display enhanced concentration of the nuclear matrix-associated protein NuMA as a result of translation from maternal mRNA and de novo transcription. The A-kinase anchoring protein 95 (AKAP95), a marker of the nuclear envelope-chromatin interface, is of somatic origin. Furthermore, greater resistance of AKAP95 and DNA to in situ extractions of one-cell stage NT embryos with non-ionic detergent, DNase, RNase and NaCl reflects an enhanced proportion of heterochromatin in these embryos. Passage through first embryonic mitosis does not rescue the defects detected in one-cell stage embryos. We propose that somatic nuclear reprogramming deficiencies by NT might emanate from, at least in part, failure to remodel the somatic nucleus morphologically into a functional embryonic nucleus.

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Bibliographic Details
Main Authors: Moreira, P. N., Robl, J. M., Collas, P.
Format: journal article biblioteca
Language:English
Published: Company of Biologists 2003
Subjects:Chromatin, Embryo, Mouse, Nuclear envelope, Nuclear transplantation,
Online Access:http://hdl.handle.net/20.500.12792/2997
http://hdl.handle.net/10261/294206
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spelling dig-inia-es-10261-2942062023-02-20T10:36:25Z Architectural defects in pronuclei of mouse nuclear transplant embryos Moreira, P. N. Robl, J. M. Collas, P. Chromatin Embryo Mouse Nuclear envelope Nuclear transplantation Reprogramming somatic nuclear function by transplantation of nuclei into recipient oocytes is associated with a morphological remodeling of the somatic nucleus. Successful cloning of animals by nuclear transplantation (NT) demonstrates that reprogramming somatic cell function is possible. However, low pregnancy rates and high frequencies of lethal abnormalities in animals born suggest that reprogramming is rarely complete. To address this issue, we tested the hypothesis that nuclear transplantation leads to nuclear remodeling deficiencies. We report the identification of several markers of morphological remodeling, or lack thereof, of mouse cumulus cell nuclei after transplantation into oocytes. Notably, nuclear transplant mouse embryos exhibit nuclear assembly of the differentiated cell-specific A-type lamins at the one-cell stage, as a result of misregulation of lamin A gene expression. The transplanted nuclei also display enhanced concentration of the nuclear matrix-associated protein NuMA as a result of translation from maternal mRNA and de novo transcription. The A-kinase anchoring protein 95 (AKAP95), a marker of the nuclear envelope-chromatin interface, is of somatic origin. Furthermore, greater resistance of AKAP95 and DNA to in situ extractions of one-cell stage NT embryos with non-ionic detergent, DNase, RNase and NaCl reflects an enhanced proportion of heterochromatin in these embryos. Passage through first embryonic mitosis does not rescue the defects detected in one-cell stage embryos. We propose that somatic nuclear reprogramming deficiencies by NT might emanate from, at least in part, failure to remodel the somatic nucleus morphologically into a functional embryonic nucleus. 2023-02-20T10:36:25Z 2023-02-20T10:36:25Z 2003 journal article Journal of Cell Science 116(18): 3713-3720 (2003) 0021-9533 http://hdl.handle.net/20.500.12792/2997 http://hdl.handle.net/10261/294206 10.1242/jcs.00692 1477-9137 en open Company of Biologists
institution INIA ES
collection DSpace
country España
countrycode ES
component Bibliográfico
access En linea
databasecode dig-inia-es
tag biblioteca
region Europa del Sur
libraryname Biblioteca del INIA España
language English
topic Chromatin
Embryo
Mouse
Nuclear envelope
Nuclear transplantation
Chromatin
Embryo
Mouse
Nuclear envelope
Nuclear transplantation
spellingShingle Chromatin
Embryo
Mouse
Nuclear envelope
Nuclear transplantation
Chromatin
Embryo
Mouse
Nuclear envelope
Nuclear transplantation
Moreira, P. N.
Robl, J. M.
Collas, P.
Architectural defects in pronuclei of mouse nuclear transplant embryos
description Reprogramming somatic nuclear function by transplantation of nuclei into recipient oocytes is associated with a morphological remodeling of the somatic nucleus. Successful cloning of animals by nuclear transplantation (NT) demonstrates that reprogramming somatic cell function is possible. However, low pregnancy rates and high frequencies of lethal abnormalities in animals born suggest that reprogramming is rarely complete. To address this issue, we tested the hypothesis that nuclear transplantation leads to nuclear remodeling deficiencies. We report the identification of several markers of morphological remodeling, or lack thereof, of mouse cumulus cell nuclei after transplantation into oocytes. Notably, nuclear transplant mouse embryos exhibit nuclear assembly of the differentiated cell-specific A-type lamins at the one-cell stage, as a result of misregulation of lamin A gene expression. The transplanted nuclei also display enhanced concentration of the nuclear matrix-associated protein NuMA as a result of translation from maternal mRNA and de novo transcription. The A-kinase anchoring protein 95 (AKAP95), a marker of the nuclear envelope-chromatin interface, is of somatic origin. Furthermore, greater resistance of AKAP95 and DNA to in situ extractions of one-cell stage NT embryos with non-ionic detergent, DNase, RNase and NaCl reflects an enhanced proportion of heterochromatin in these embryos. Passage through first embryonic mitosis does not rescue the defects detected in one-cell stage embryos. We propose that somatic nuclear reprogramming deficiencies by NT might emanate from, at least in part, failure to remodel the somatic nucleus morphologically into a functional embryonic nucleus.
format journal article
topic_facet Chromatin
Embryo
Mouse
Nuclear envelope
Nuclear transplantation
author Moreira, P. N.
Robl, J. M.
Collas, P.
author_facet Moreira, P. N.
Robl, J. M.
Collas, P.
author_sort Moreira, P. N.
title Architectural defects in pronuclei of mouse nuclear transplant embryos
title_short Architectural defects in pronuclei of mouse nuclear transplant embryos
title_full Architectural defects in pronuclei of mouse nuclear transplant embryos
title_fullStr Architectural defects in pronuclei of mouse nuclear transplant embryos
title_full_unstemmed Architectural defects in pronuclei of mouse nuclear transplant embryos
title_sort architectural defects in pronuclei of mouse nuclear transplant embryos
publisher Company of Biologists
publishDate 2003
url http://hdl.handle.net/20.500.12792/2997
http://hdl.handle.net/10261/294206
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AT robljm architecturaldefectsinpronucleiofmousenucleartransplantembryos
AT collasp architecturaldefectsinpronucleiofmousenucleartransplantembryos
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