𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Expression of methylation pathway enzymes in bovine oocytes and preimplantation embryos

✍ Scribed by Shuntaro Ikeda; Takahiro Namekawa; Miki Sugimoto; Shin-ichi Kume


Publisher
Wiley (John Wiley & Sons)
Year
2010
Tongue
English
Weight
432 KB
Volume
9999A
Category
Article
ISSN
1932-5223

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

The methylation pathway, which consists of two metabolic cycles of nutrients, i.e., the methionine and folate cycles, generates S‐adenosylmethionine, the methyl donor for the methylation of DNA and histones. Using reverse transcription‐polymerase chain reaction, we examined the gene expression patterns of the methylation pathway enzymes during bovine oocyte maturation and preimplantation embryonic development up to the blastocyst stage. Bovine oocytes were demonstrated to have the mRNA of all methylation pathway enzymes examined, namely, methionine adenosyltransferase 1A (MAT1A), MAT2A, MAT2B, S‐adenosylhomocysteine hydrolase (AHCY), 5‐methyltetrahydrofolate‐homocysteine methyltransferase (MTR), betaine‐homocysteine methyltransferase (BHMT), serine hydroxymethyltransferase 1 (SHMT1), SHMT2, and 5,10‐methylenetetrahydrofolate reductase (MTHFR). All the transcripts were consistently expressed throughout all developmental stages, except for MAT1A, which was not detected from the 8‐cell stage onward and BHMT, which was not detected in the 8‐cell stage. Immunofluorescence analysis of MAT1A protein revealed the relatively higher expression in oocytes and early cleavage stage embryos up to the 8‐cell stage compared with the morula and blastocyst stage. Further, to investigate the effects of methylation pathway disruption during the earliest stages of embryonic development, the effects of exogenous homocysteine on preimplantation development and DNA methylation of bovine embryos were investigated in vitro. As results, high concentrations of homocysteine induced hypermethylation of genomic DNA as well as developmental retardation in bovine embryos. These results provide a new insight into nutrient‐sensitive epigenetic regulation and perturbation at the earliest stage of our life. J. Exp. Zool. 313A:129–136, 2010. © 2010 Wiley‐Liss, Inc.


📜 SIMILAR VOLUMES


Glucose transporter expression is develo
✍ Robert Augustin; Paola Pocar; Anne Navarrete-Santos; Christine Wrenzycki; Fulvio 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 165 KB

## Abstract Glucose is readily been taken up and utilized by preimplantation embryos from different species. However, a comprehensive analysis of the glucose transporter expression throughout preimplantation development is still missing. Here, we have investigated the expression of facilitative glu

Expression of homeobox-containing genes
✍ Siriluck Ponsuksili; Klaus Wimmers; James Adjaye; Karl Schellander 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 140 KB

## Abstract The homeobox‐containing gene family plays a pivotal role in regulating, patterning, and axial morphogenesis in the developing embryo. But there is still very little known about the expression and function of these genes in mammalian oocytes and preimplantation stage embryos. In this stu

The expression of genes in human preimpl
✍ Eugene Pergament; Morris Fiddler 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 173 KB 👁 2 views

The study of gene expression in human preimplantation embryos is establishing itself as a necessary dimension of developmental biology and medical genetics. Transcripts identified in human preimplantation embryos include housekeeping genes, transcription and growth factor genes, sex-determining gene

Expression of interleukin-6 in porcine,
✍ Dr. Nagappan Mathialagan; James A. Bixby; R. Michael Roberts 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 711 KB

## Abstract A porcine interleukin‐6 (pIL6) cDNA has been cloned from pig spleen cDNA library to provide information that would allow us to study IL‐6 mRNA expression during pregnancy of several domestic Artiodactyla. The cDNA is 1058 bp long and with a single open reading frame that encodes a 212 a