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通过测量单个卵裂球中X连锁基因剂量对植入前小鼠胚胎进行性别鉴定。

Sexing of preimplantation mouse embryos by measurement of X-linked gene dosage in a single blastomere.

作者信息

Monk M, Handyside A H

机构信息

MRC Mammalian Development Unit, London, U.K.

出版信息

J Reprod Fertil. 1988 Jan;82(1):365-8. doi: 10.1530/jrf.0.0820365.

Abstract

Single blastomeres were isolated from zona-free 8-cell mouse embryos and assayed for X-linked hypoxanthine phosphoribosyl transferase (HPRT) activity and autosome-linked adenine phosphoribosyl transferase (APRT) activity. At this stage of development both X chromosomes are active in female embryos. Hence, a bimodal distribution of HPRT: APRT ratios, corresponding to male (XY) and female (XX) biopsied samples, was observed due to the 2-fold difference in gene dosage for HPRT activity. Batches of putative male and female embryos identified in this way were transferred to pseudopregnant recipient females. Development of the seven-eighths embryos was equivalent to that of control zona-free intact embryos. Sex determination by measurement of X-linked gene dosage was accurate and rapid enough to allow transfer of embryos of known sex without the need for cryopreservation.

摘要

从无透明带的8细胞小鼠胚胎中分离出单个卵裂球,并检测其X连锁次黄嘌呤磷酸核糖转移酶(HPRT)活性和常染色体连锁腺嘌呤磷酸核糖转移酶(APRT)活性。在发育的这个阶段,雌性胚胎中的两条X染色体都是活跃的。因此,由于HPRT活性的基因剂量存在2倍差异,观察到HPRT:APRT比值呈双峰分布,分别对应雄性(XY)和雌性(XX)活检样本。以这种方式鉴定出的一批假定的雄性和雌性胚胎被移植到假孕受体雌性体内。八分之七的胚胎发育情况与对照无透明带完整胚胎相当。通过测量X连锁基因剂量进行性别鉴定足够准确和快速,无需冷冻保存即可移植已知性别的胚胎。

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