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1.
Epigenomics ; 11(5): 543-561, 2019 04.
Artículo en Inglés | MEDLINE | ID: mdl-30667280

RESUMEN

AIMS: Epigenetic signatures of germline cells are dynamically reprogrammed to induce appropriate differentiation, development and sex specification. We investigated sex-specific epigenetic changes in mouse fetal germ cells (FGCs) and neonatal germ cells. MATERIALS & METHODS: Six histone marks in mouse E13.5 FGCs and P1 neonatal germ cells were analyzed by chromatin immunoprecipitation and sequencing. These datasets were compared with transposase-accessible chromatin sites, DNA methylation and transcriptome. RESULTS: Different patterns of each histone mark were detected in female and male FGCs, and H3K4me3/H3K27me3 bivalent marks were enriched in different chromosomal regions of female and male FGCs. CONCLUSION: Our results suggest that histone modifications may affect FGC gene expression following DNA methylation erasure, contributing to the differentiation into female and male germ cells.


Asunto(s)
Células Germinativas/metabolismo , Histonas/metabolismo , Animales , Animales Recién Nacidos , Epigenómica , Femenino , Feto/citología , Células Germinativas/citología , Masculino , Metilación , Ratones , Ratones Endogámicos C57BL , Transcriptoma
2.
Biol Reprod ; 94(6): 128, 2016 06.
Artículo en Inglés | MEDLINE | ID: mdl-27103445

RESUMEN

The germ line reprogramming barrier resets parental epigenetic modifications according to sex, conferring totipotency to mammalian embryos upon fertilization. However, it is not known whether epigenetic errors are committed during germ line reprogramming that are then transmitted to germ cells, and consequently to offspring. We addressed this question in the present study by performing a genome-wide DNA methylation analysis using a target postbisulfite sequencing method in order to identify DNA methylation errors in cloned mouse sperm. The sperm genomes of two somatic cell-cloned mice (CL1 and CL7) contained significantly higher numbers of differentially methylated CpG sites (P = 0.0045 and P = 0.0116). As a result, they had higher numbers of differentially methylated CpG islands. However, there was no evidence that these sites were transmitted to the sperm genome of offspring. These results suggest that DNA methylation errors resulting from embryo cloning are transmitted to the sperm genome by evading the germ line reprogramming barrier.


Asunto(s)
Clonación de Organismos , Metilación de ADN , Epigénesis Genética , Espermatozoides/metabolismo , Animales , Masculino , Ratones , Ratones Endogámicos C57BL , Ratones Endogámicos DBA
3.
PLoS One ; 10(12): e0144836, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26700643

RESUMEN

In mice, primordial germ cells migrate into the genital ridges by embryonic day 13.5 (E13.5), where they are then subjected to a sex-specific fate with female and male primordial germ cells undergoing mitotic arrest and meiosis, respectively. However, the sex-specific basis of primordial germ cell differentiation is poorly understood. The aim of this study was to investigate the sex-specific features of mouse primordial germ cells. We performed RNA-sequencing (seq) of E13.5 female and male mouse primordial germ cells using next-generation sequencing. We identified 651 and 428 differentially expressed transcripts (>2-fold, P < 0.05) in female and male primordial germ cells, respectively. Of these, many transcription factors were identified. Gene ontology and network analysis revealed differing functions of the identified female- and male-specific genes that were associated with primordial germ cell acquisition of sex-specific properties required for differentiation into germ cells. Furthermore, DNA methylation and ChIP-seq analysis of histone modifications showed that hypomethylated gene promoter regions were bound with H3K4me3 and H3K27me3. Our global transcriptome data showed that in mice, primordial germ cells are decisively assigned to a sex-specific differentiation program by E13.5, which is necessary for the development of vital germ cells.


Asunto(s)
Biomarcadores/metabolismo , Diferenciación Celular/genética , Metilación de ADN , Regulación del Desarrollo de la Expresión Génica , Células Germinativas/metabolismo , Animales , Inmunoprecipitación de Cromatina , Femenino , Células Germinativas/citología , Secuenciación de Nucleótidos de Alto Rendimiento/métodos , Histonas/metabolismo , Masculino , Ratones , Ratones Endogámicos C57BL , Análisis de Componente Principal , Factores Sexuales , Análisis de la Célula Individual/métodos
4.
Stem Cells ; 29(9): 1362-70, 2011 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-21732496

RESUMEN

c-Myc transduction has been considered previously to be nonessential for induced pluripotent stem cell (iPSC) generation. In this study, we investigated the effects of c-Myc transduction on the generation of iPSCs from an inbred mouse strain using a genome integration-free vector to exclude the effects of the genetic background and the genomic integration of exogenous genes. Our findings reveal a clear difference between iPSCs generated using the four defined factors including c-Myc (4F-iPSCs) and those produced without c-Myc (3F-iPSCs). Molecular and cellular analyses did not reveal any differences between 3F-iPSCs and 4F-iPSCs, as reported previously. However, a chimeric mice formation test indicated clear differences, whereby few highly chimeric mice and no germline transmission was observed using 3F-iPSCs. Similar differences were also observed in the mouse line that has been widely used in iPSC studies. Furthermore, the defect in 3F-iPSCs was considerably improved by trichostatin A, a histone deacetyl transferase inhibitor, indicating that c-Myc plays a crucial role in iPSC generation through the control of histone acetylation. Indeed, low levels of histone acetylation were observed in 3F-iPSCs. Our results shed new light on iPSC generation mechanisms and strongly recommend c-Myc transduction for preparing high-quality iPSCs.


Asunto(s)
Células Madre Pluripotentes Inducidas/fisiología , Proteínas Proto-Oncogénicas c-myc/genética , Animales , Blastómeros/fisiología , Quimera , Células Madre Embrionarias/citología , Células Madre Embrionarias/fisiología , Femenino , Genes myc , Células Madre Pluripotentes Inducidas/citología , Células Madre Pluripotentes Inducidas/metabolismo , Masculino , Ratones , Ratones Endogámicos C57BL , Embarazo , Proteínas Proto-Oncogénicas c-myc/biosíntesis , Transducción Genética
5.
PLoS One ; 5(6): e11274, 2010 Jun 30.
Artículo en Inglés | MEDLINE | ID: mdl-20614022

RESUMEN

Although cloned embryos generated by somatic/embryonic stem cell nuclear transfer (SECNT) certainly give rise to viable individuals, they can often undergo embryonic arrest at any stage of embryogenesis, leading to diverse morphological abnormalities. In an effort to gain further insights into reprogramming and the properties of SECNT embryos, we performed a large-scale gene expression profiling of 87 single blastocysts using GeneChip microarrays. Sertoli cells, cumulus cells, and embryonic stem cells were used as donor cells. The gene expression profiles of 87 blastocysts were subjected to microarray analysis. Using principal component analysis and hierarchical clustering, the gene expression profiles were clearly classified into 3 clusters corresponding to the type of donor cell. The results revealed that each type of SECNT embryo had a unique gene expression profile that was strictly dependent upon the type of donor cells, although there was considerable variation among the individual profiles within each group. This suggests that the reprogramming process is distinct for embryos cloned from different types of donor cells. Furthermore, on the basis of the results of comparison analysis, we identified 35 genes that were inappropriately reprogrammed in most of the SECNT embryos; our findings demonstrated that some of these genes, such as Asz1, Xlr3a and App, were appropriately reprogrammed only in the embryos with a transcriptional profile that was the closest to that of the controls. Our findings provide a framework to further understand the reprogramming in SECNT embryos.


Asunto(s)
Blastocisto/metabolismo , Perfilación de la Expresión Génica , Animales , Blastocisto/citología , Clonación de Organismos , Regulación hacia Abajo , Ratones , Análisis de Secuencia por Matrices de Oligonucleótidos , Reacción en Cadena de la Polimerasa , Regulación hacia Arriba
6.
J Biol Chem ; 285(34): 26384-9, 2010 Aug 20.
Artículo en Inglés | MEDLINE | ID: mdl-20554535

RESUMEN

Although the induction of genome integration-free induced pluripotent stem cells (iPSCs) has been reported, c-Myc was still required for the efficient generation of these cells. Herein, we report mouse strain-dependent differences in the c-Myc dependence for iPSC generation and the successful generation of genome integration-free iPSCs without c-Myc transduction using C57BL/6 mouse embryonic fibroblasts. We performed 49 independent experiments and obtained a total of 24 iPSC clones, including 18 genome integration-free iPSC clones. These iPSCs were indistinguishable from embryonic stem cells and from iPSCs generated using other methods. Furthermore, the generation of three-factor iPSCs free of virus vectors revealed the contribution of c-Myc to the genomic integration of external genes. C57BL/6 is an inbred mouse strain with substantial advantages for use in genetic and molecular biological studies due to its use in the whole mouse genome sequencing project. Thus, the present series of C57BL/6 iPSCs generated by various procedures will serve as a valuable resource for future genetic studies of iPSC generation.


Asunto(s)
Fibroblastos/citología , Células Madre Pluripotentes Inducidas/citología , Proteínas Proto-Oncogénicas c-myc/farmacología , Animales , Técnicas de Cultivo de Célula , Células Clonales/citología , Células Madre Embrionarias/citología , Métodos , Ratones , Especificidad de la Especie , Transducción Genética
7.
Stem Cells ; 28(2): 213-20, 2010 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-20020427

RESUMEN

The emergence of induced pluripotent stem cells (iPSCs) from an ancestral somatic cell is one of the most important processes underlying their generation, but the mechanism has yet to be identified. This is principally because these cells emerge at a low frequency, about 0.1% in the case of fibroblasts, and in a stochastic manner. In our current study, we succeeded in identifying ancestral fibroblasts and the subsequent processes leading to their conversion to iPSCs. The ancestral fibroblasts were found to divide several times in a morphologically symmetric manner, maintaining a fibroblastic shape, and then gradually transform into embryonic stem-like cells. Interestingly, this conversion occurred within 48 hours after gene introduction in most iPSC generations. This is the first report to directly observe a cell lineage conversion of somatic cells to stem cells and provides a critical new insight into the "black box" of iPSCs, that is, the first three days of their generation.


Asunto(s)
Fibroblastos/citología , Células Madre Pluripotentes Inducidas/citología , Animales , Células Cultivadas , Fibroblastos/metabolismo , Células Madre Pluripotentes Inducidas/metabolismo , Ratones , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa
8.
Biol Reprod ; 78(4): 568-76, 2008 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-17978277

RESUMEN

During development, cloned embryos often undergo embryonic arrest at any stage of embryogenesis, leading to diverse morphological abnormalities. The long-term effects resulting from embryo cloning procedures would manifest after birth as early death, obesity, various functional disorders, and so forth. Despite extensive studies, the parameters affecting the developmental features of cloned embryos remain unclear. The present study carried out extensive gene expression analysis to screen a cluster of genes aberrantly expressed in embryonic stem cell-cloned blastocysts. Differential screening of cDNA subtraction libraries revealed 224 differentially expressed genes in the cloned blastocysts: eighty-five were identified by the BLAST search as known genes performing a wide range of functions. To confirm their differential expression, quantitative gene expression analyses were performed by real-time PCR using single blastocysts. The genes Skp1a, Canx, Ctsd, Timd2, and Psmc6 were significantly up-regulated, whereas Aqp3, Ak3l1, Rhot1, Sf3b3, Nid1, mt-Rnr2, mt-Nd1, mt-Cytb, and mt-Co2 were significantly down-regulated in the majority of embryonic stem cell-cloned embryos. Our results suggest that an extraordinarily high frequency of multiple functional disorders caused by the aberrant expression of various genes in the blastocyst stage is involved in developmental arrest and various other disorders in cloned embryos.


Asunto(s)
Blastocisto/química , Clonación de Organismos , Células Madre Embrionarias/química , Expresión Génica , Animales , Clonación Molecular , ADN Complementario/análisis , ADN Complementario/química , Femenino , Regulación del Desarrollo de la Expresión Génica , Ratones , Ratones Endogámicos C57BL , Ratones Endogámicos DBA , Reacción en Cadena de la Polimerasa
9.
Biochem Biophys Res Commun ; 297(2): 323-8, 2002 Sep 20.
Artículo en Inglés | MEDLINE | ID: mdl-12237121

RESUMEN

The IF3 gene was isolated by expression cloning from a cDNA library of mouse oocytes. This gene was revealed to have no homology to any known gene and its cDNA encodes a 202-amino acid protein that contains a signal-peptide sequence. Moreover, an IF3 isoform, IF3(2), was expressed in both liver and ovary. Its cDNA encoded a 92-amino acid protein contains a signal-peptide sequence, which may be an alternative splice and frameshift form of IF3. The mRNA of IF3s was expressed in oocytes, ovary, and liver. Moreover, the gene expression of IF3s was regulated in a development-dependent manner in preimplantation-embryo and liver. Both IF3(1) and IF3(2) isoforms induced the differentiation of 2T3 and ATDC5 cells to the osteogenic and chondrogenic phenotype, respectively, suggesting that IF3s may modulate the differentiation status. Our findings suggest that IF3 may be one of the secreted factors that regulate oogenesis and certain liver functions.


Asunto(s)
Diferenciación Celular/fisiología , Hígado/metabolismo , Ovario/metabolismo , Proteínas/metabolismo , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Línea Celular , Femenino , Biblioteca de Genes , Masculino , Ratones , Ratones Endogámicos C57BL , Datos de Secuencia Molecular , Oocitos/química , Oocitos/metabolismo , Isoformas de Proteínas , Señales de Clasificación de Proteína , Proteínas/química , Proteínas/genética , Distribución Tisular
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