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用于生产绿色荧光蛋白表达水牛(Bubalus bubalis)胚胎的原核DNA显微注射技术的开发。

Development of a pronuclear DNA microinjection technique for production of green fluorescent protein-expressing bubaline (Bubalus bubalis) embryos.

作者信息

Verma V, Gautam S K, Palta P, Manik R S, Singla S K, Chauhan M S

机构信息

Animal Biotechnology Centre, National Dairy Research Institute, Karnal, Haryana 132001, India.

出版信息

Theriogenology. 2008 Apr 1;69(6):655-65. doi: 10.1016/j.theriogenology.2007.09.035. Epub 2008 Feb 12.

Abstract

Oocytes from abattoir-derived bubaline (Bubalus bubalis) ovaries were subjected to IVM and IVF; the objective was to develop a pronuclear DNA microinjection technique to produce embryos expressing green fluorescent protein (GFP). The largest proportion (61.2%) of zygotes in which one (1 PN) or two pronuclei (2 PN) were visible was when centrifugation (14,000 x g for 15 min) was done 16 h after insemination. Centrifugation had no adverse effects on cleavage rate, development to morulae/blastocysts, and total cell number of embryos. Piercing the pronuclear but not the plasma membrane reduced (P<0.05) cleavage rate (44.0% vs. 51.0%), without affecting subsequent development. Following microinjection of a GFP-DNA construct, cleavage rate (55.9, 38.9, and 30.9%) and proportion of cleaved embryos that developed to morulae (39.9, 25.6, and 15.5%) and blastocyst stages (22.4, 13.4, and 2.8%) were higher (P<0.05) for non-injected controls than for those injected with buffer alone, which, in turn, were higher (P<0.05) than for those injected with buffer containing 5 microg/mL DNA. The cleavage rate (39.2% vs. 34.8%) and proportion of cleaved embryos that developed to morulae/blastocysts (37.5% vs. 10.9%) were higher (P<0.05) for microinjected zygotes with 2 PN than for those with 1 PN. The cleavage rate and the proportion of cleaved embryos that developed to morulae and blastocysts were higher (P<0.05) following culture of microinjected zygotes in mCR2aa medium (40.7, 32.7, and 9.1%, respectively) compared to those for mSOFaa (33.3, 26.0, and 6.5%, respectively) or after culture in TCM-199+co-culture with buffalo oviductal epithelial cells (31.2, 25.0, and 4.5%, respectively). The proportion of embryos expressing GFP was higher (P<0.01) for 2 PN than for 1 PN zygotes (15.9% vs. 13.7%). Thirty-five embryos expressed GFP; the proportion of mosaic embryos (62.8%) was higher (P<0.01) than of embryos in which all blastomeres expressed GFP (37.2%); eight and two of those embryos developed to the morula and blastocyst stages, respectively.

摘要

对来自屠宰场水牛奶牛(水牛属水牛)卵巢的卵母细胞进行体外成熟(IVM)和体外受精(IVF);目的是开发一种原核DNA显微注射技术来生产表达绿色荧光蛋白(GFP)的胚胎。在授精后16小时进行离心(14,000×g,15分钟)时,可见一个原核(1PN)或两个原核(2PN)的受精卵比例最高(61.2%)。离心对胚胎的卵裂率、发育至桑葚胚/囊胚的情况以及总细胞数没有不良影响。穿刺原核而非质膜会降低(P<0.05)卵裂率(44.0%对51.0%),但不影响后续发育。在显微注射GFP - DNA构建体后,未注射的对照组的卵裂率(55.9%、38.9%和30.9%)以及发育至桑葚胚(39.9%、25.6%和15.5%)和囊胚阶段(22.4%、13.4%和2.8%)的卵裂胚胎比例高于单独注射缓冲液的组(P<0.05),而单独注射缓冲液的组又高于注射含5μg/mL DNA缓冲液的组(P<0.05)。具有2PN的显微注射受精卵的卵裂率(39.2%对34.8%)以及发育至桑葚胚/囊胚的卵裂胚胎比例(37.5%对10.9%)高于具有1PN的受精卵(P<0.05)。与在mSOFaa培养基中培养(分别为33.3%、26.0%和6.5%)或在TCM - 199中与水牛输卵管上皮细胞共培养后(分别为31.2%、25.0%和4.5%)相比,在mCR2aa培养基中培养显微注射受精卵后,卵裂率以及发育至桑葚胚和囊胚的卵裂胚胎比例更高(P<0.05)(分别为40.7%、3,27%和9.1%)。2PN受精卵表达GFP的胚胎比例高于1PN受精卵(15.9%对13.7%,P<0.01)。35个胚胎表达了GFP;镶嵌胚胎比例(62.8%)高于所有卵裂球都表达GFP的胚胎(37.2%,P<0.01);其中8个和2个胚胎分别发育至桑葚胚和囊胚阶段。

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