Subsets of cloned mouse embryos and their non-random relationship to development and nuclear reprogramming.

Abstract:

:An important question in oocyte-mediated nuclear reprogramming is whether gene expression of the donor nucleus changes randomly or follows a pattern. Since cloned embryos are very heterogeneous and arrest frequently during preimplantation development, a random scenario is generally accepted. In the present study, we resolve the heterogeneity of cumulus cell-derived mouse clones by recognizing structured subsets, and we analyze their relationship to reprogramming of donor nuclei. We utilize live cell imaging of the Oct4 promoter-driven GFP transgene to resolve the populations of cloned and ICSI-fertilized morulae, and we sort them both into three subsets based on different GFP expression. Functionally, subsets of cloned but not ICSI morulae form blastocysts and ES cells proportional to Oct4-GFP expression. Regulatively, the subsets of cloned morulae are characterized by small differences of transcript level for the pluripotency-associated genes Oct4, Nanog and Sox2. Small differences of the level of select mRNAs across subsets suggest a uniform rather than random course of reprogramming from the morula stage on. Since these small differences correspond with substantial differences in developmental competence, we propose that developmental potential of clones relates to levels of gene expression in a different way than fertilized embryos.

journal_name

Mech Dev

authors

Cavaleri FM,Balbach ST,Gentile L,Jauch A,Böhm-Steuer B,Han YM,Schöler HR,Boiani M

doi

10.1016/j.mod.2007.09.007

subject

Has Abstract

pub_date

2008-01-01 00:00:00

pages

153-66

issue

1-2

eissn

0925-4773

issn

1872-6356

pii

S0925-4773(07)00155-4

journal_volume

125

pub_type

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