首页> 外文OA文献 >Heteroplasmy in bovine fetuses produced by intra and inter subspecific somatic cell nuclear transfer: Neutral segregation of nuclear donor mitochondrial DNA in various tissues and evidence for recipient cow mitochondria in fetal blood.
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Heteroplasmy in bovine fetuses produced by intra and inter subspecific somatic cell nuclear transfer: Neutral segregation of nuclear donor mitochondrial DNA in various tissues and evidence for recipient cow mitochondria in fetal blood.

机译:通过内部和亚种间体细胞核转移产生的牛胎儿的异质性:各种组织中核供体线粒体DNa的中性分离和胎儿血液中受体牛线粒体的证据。

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摘要

Varying degrees of mitochondrial DNA (mtDNA) heteroplasmy have been observed in nuclear transfer embryos, fetuses, and offspring, but the mechanisms leading to this condition are unknown. We have generated a clone of 12 bovine somatic cell nuclear transfer fetuses, using nuclear donor cells, recipient oocytes, and recipient heifers with defined mtDNA genotypes, to study nuclear-mitochondrial interactions and the origins of mtDNA heteroplasmy. Embryos were reconstructed from granulosa cells with Bos taurus mtDNA type A and recipient oocytes collected from three different maternal lineages with B. taurus mtDNA type B, B. taurus mtDNA type C, or B. indicus mtDNA. Sequence differences in the control region (CR) of B. taurus mtDNAs ranged from 6 to 11 nucleotides and differences between B. taurus and B. indicus CRs from 45 to 50 nucleotides. Fetuses were recovered from recipient heifers with B. taurus mtDNA type B on Day 80 after nuclear transfer (eight B. taurus A/B, two B. taurus A/C, and two B. taurus A/B. indicus). Agarose gel analysis of the CR by polymerase chain reaction-based restriction fragment length polymorphism failed to detect nuclear donor mtDNA in 11 investigated tissues of 10 viable fetuses and in DNA samples of two fetuses in resorption (one B. taurus A/B and one B. taurus A/C). A more sensitive analysis of 1801 plasmid clones with CR inserts derived from tissues of a B. taurus A/B. indicus fetus detected no or very low levels of heteroplasmy (0.5–0.7%). However, the analyses detected considerable amounts (~2.5% and 5%) of recipient heifer mtDNA in blood samples from two fetuses. Our data do not suggest a replicative advantage of somatic nuclear donor cell mtDNA in bovine transmitochondrial clones produced with oocytes from domestic forms of the same or a different aurochs (B. primigenius) subspecies. Detection of mtDNA from the recipient animal in the circulation of two fetuses points to leakage of the placental barrier, mimicking heteroplasmy.
机译:在核移植胚胎,胎儿和后代中观察到不同程度的线粒体DNA(mtDNA)异质性,但导致这种情况的机理尚不清楚。我们使用核供体细胞,受体卵母细胞和具有定义的mtDNA基因型的受体小母牛生成了12个牛体细胞核移植胎儿的克隆,以研究核-线粒体相互作用和mtDNA异质性的起源。从具有Bos taurus mtDNA A型的颗粒细胞和从三个不同的母体谱系B. taurus mtDNA B,B。taurus mtDNA C或B. indicus mtDNA收集的受体卵母细胞中重建胚胎。金牛座牛的mtDNA的控制区(CR)的序列差异为6至11个核苷酸,金牛座牛和印度产的B. indicus CR之间的序列差异为45至50个核苷酸。核移植后第80天,从接受牛的牛具有mtDNA B型牛(B. taurus mtDNA)中回收胎儿(八个B. taurus A / B,两个B. taurus A / C和两个B. taurus A / B。indicus)。通过基于聚合酶链反应的限制性片段长度多态性对CR进行琼脂糖凝胶分析,未能在10个存活胎儿的11个被调查组织中以及两个胎儿吸收的DNA样本中检测到一个核供体mtDNA(一个B. taurus A / B和一个B.金牛座A / C)。对带有金牛芽孢杆菌A / B组织CR插入片段的1801质粒克隆进行更灵敏的分析。胎儿未检测到异质性或异质性水平很低(0.5-0.7%)。但是,分析检测到来自两个胎儿的血液样本中有相当数量(〜2.5%和5%)的受体小母牛mtDNA。我们的数据没有表明体细胞供体细胞mtDNA在由来自相同或不同的金龟子(B. primigenius)亚种的家养形式的卵母细胞产生的牛透射线粒体克隆中的复制优势。在两个胎儿的循环中检测到来自受体动物的mtDNA,这表明胎盘屏障的泄漏,模仿了异质性。

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