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Expression of β-galactosidase in preimplantation ovine and porcine embryos

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TLDR
expression of lysosomal β-galactosidase in ovine and porcine preimplantation embryos followed a similar rate of increase as that described for murine embryos.
Abstract
Knowledge regarding the timing of embryonic expression of the mammalian genome is of relevance for the development of preimplantation diagnostic methods for human genetic diseases. For development of preimplantation diagnosis of lysosomal storage diseases, it will be necessary to know at which embryonic stage the genes for lysosomal enzymes are expressed. In previous studies by other investigators, it has been shown that lysosomal alpha- and beta-galactosidase and beta-glucuronidase in murine embryos increase 50- to 100-fold in activity between the two-cell and late blastocyst stage. We describe here expression of lysosomal beta-galactosidase in preimplantation ovine (two-cell through midblastocyst) and porcine (two-cell through late blastocyst) embryos. Expression of beta-galactosidase in ovine and porcine preimplantation embryos followed a similar rate of increase as that described for murine embryos. Activity of beta-galactosidase increased over 10-fold between the two- to four-cell and midblastocyst stages in ovine embryos, and 300-fold between the two- to four-cell and late blastocyst stages in porcine embryos. Activity expressed on a per cell basis was relatively constant in ovine embryos, as has been described in murine embryos, and increased approximately 5-fold on a per cell basis in porcine embryos. Activity of beta-galactosidase in ovine and porcine embryos initially was greater than 12-fold on a per cell or per embryo basis than in murine embryos evaluated. The knowledge of beta-galactosidase embryonic expression may provide the basis for preimplantation diagnosis of genetic beta-galactosidase deficiency in these species.

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Journal ArticleDOI

Comparative proteomic and regulatory network analyses of the elongating pig conceptus

TL;DR: A comparison of the protein expression profile with transcriptomic data from pig concepti of the same developmental stages identified similarities and dissimilarities between protein and mRNA expression profiles.
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beta-galactosidase transduced T lymphocytes: a comparison between stimulation by either PHA and IL-2 or a mixed lymphocyte reaction.

TL;DR: The results indicate that: a) the use of FLac or NuNL vector retroviral-mediated gene transfer into T-lymphocytes derived from peripheral blood and stimulated by either PHA/IL-2 or a MLR produces a high percentage of transduced T cells; b) MLR is a good system for generating a transduces alloreactive lymphocyte population.
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Ovine GM-1 gangliosidosis.

TL;DR: The described disease emphasizes the importance of clinical and pathologic evaluation of neonatal deaths as the economic and research importance of genetic diseases are unrealized.
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Developmental changes in the fetal pig transcriptome.

TL;DR: Novel transcriptome changes in fetal pigs during a period of rapid growth involved genes with a spectrum of proposed functions, including musculoskeletal growth, immune system function, and cellular regulation.
References
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Journal ArticleDOI

Human gene expression first occurs between the four- and eight-cell stages of preimplantation development

TL;DR: Changes in the pattern of polypeptides synthesized during the pre-implantation stages of human development are described, and it is demonstrated that some of the major qualitative changes which occur between the four- and eight-cell stages are dependent on transcription.
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Nuclear transplantation in the mouse embryo by microsurgery and cell fusion.

TL;DR: Nuclear transplantation in the mouse embryo was achieved by using a method that combines microsurgical removal of the zygote pronuclei with the introduction of a donor nucleus by a virus-mediated cell fusion technique.
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Heat shock proteins, first major products of zygotic gene activity in mouse embryo

TL;DR: It is shown that the 70K early two-cell-specific proteins are identical to two of the mouse heat shock proteins, HSP 68 and HSP 70.
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The relationship between cleavage, DNA replication, and gene expression in the mouse 2-cell embryo.

TL;DR: It is established that DNA replication takes place over the period 1 to 5.5 h after the first cleavage division, and that neither DNA replication nor the loss of maternal mRNA that take place during the 2-cell stage are dependent upon synthesis of the alpha-amanitin-sensitive polypeptides.
Journal ArticleDOI

Control of protein synthesis during early cleavage of sheep embryos

TL;DR: The results indicate that the full activation of transcription in sheep embryos occurs in the 4th cell cycle, and that a consistent pattern of proteins was synthesized during the first 3 cell cycles after fertilization followed by major changes in subsequent cycles.
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