Abstract

Nuclear transfer consists in injecting a somatic nucleus carrying valuable genetic information into a recipient oocyte to sire a diploid offspring which bears the genome of interest. It requires that the oocyte (maternal) DNA is removed. In fish, because enucleation is difficult to achieve, non-enucleated oocytes are often used and disappearance of the maternal DNA was reported in some clones. The present work explores which cellular events explain spontaneous erasure of maternal DNA, as mastering this phenomenon would circumvent the painstaking procedure of fish oocyte enucleation. The fate of the somatic and maternal DNA during oocyte activation and first cell cycle was studied using DNA labeling and immunofluorescence in goldfish clones. Maternal DNA was always found as an intact metaphase within the oocyte, and polar body extrusion was minimally affected after oocyte activation. During the first cell cycle, only 40% of the clones displayed symmetric cleavage, and these symmetric clones contributed to 80% of those surviving at hatching. Maternal DNA was often fragmented and located under the cleavage furrow. The somatic DNA was organized either into a normal mitotic spindle or abnormal multinuclear spindle. Scenarios matching the DNA behavior and the embryo fate are proposed.

Highlights

  • Nuclear transfer consists in injecting a somatic nucleus carrying valuable genetic information into a recipient oocyte to sire a diploid offspring which bears the genome of interest

  • In 100% of control oocytes (n = 18), maternal DNA was not found at the bottom of the micropyle, but against the side of the micropylar canal, in the ooplasm, and it was always organized in a metaphase plate (Fig. 1C)

  • This study showed that prior to activation of embryonic development, the maternal DNA at MII stage remained undisturbed by the injection procedure of Somatic cell nuclear transfer (SCNT)

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Summary

Introduction

Nuclear transfer consists in injecting a somatic nucleus carrying valuable genetic information into a recipient oocyte to sire a diploid offspring which bears the genome of interest. It requires that the oocyte (maternal) DNA is removed. Somatic cell nuclear transfer (SCNT) consists in injecting a donor somatic nucleus into a recipient oocyte to obtain a clone that carries the genome of the donor animal[1,2,3] This technology allows the restoration of valuable genetic resources from somatic material when both sperm and oocytes, or embryos, are unavailable. It is interesting that in goldfish, zebrafish, weatherfish and medaka, such a protocol avoiding the enucleation step still allows the development of clones carrying only the genome of the donor[16,17,18,19,20,21]

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