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在来自单个人类植入前胚胎的高质量cDNA文库中检测到的特定基因的发育表达。

Developmental expression of specific genes detected in high-quality cDNA libraries from single human preimplantation embryos.

作者信息

Adjaye J, Bolton V, Monk M

机构信息

Molecular Embryology Unit, Institute of Child Health, 30 Guilford Street, London, UK.

出版信息

Gene. 1999 Sep 17;237(2):373-83. doi: 10.1016/s0378-1119(99)00329-7.

Abstract

We describe an improved highly sensitive method for generating cDNA libraries containing a high proportion of cDNAs enriched with 5'-coding sequences from single human preimplantation embryos and a 10 week old whole foetus. The embryonic mRNA was isolated using oligo-(dT) linked to magnetic beads. First-strand cDNA synthesis was carried out directly on the bound mRNA, followed by PCR designed to amplify the cDNA molecules synthesized in their entirety. The complexities of the libraries are between 10(5) and 10(6) independent clones. The average cDNA size is 1.0 kb, and the size range is 0.5-3.0 kb. PCR analysis of the embryonic libraries for specific genes has revealed transcripts for genes known to be transcribed in preimplantation stages, such as the imprinted gene SNRPN, developmental genes WNT11, HOX, OCT-1 and the embryonic OCT-4, cytoskeletal genes keratin-18 and beta-actin, the cell cycle gene C-MOS, and housekeeping genes GAPDH and HPRT. Sequencing of random clones showed the presence of a variety of sequences, such as human chorionic gonadotrophin, ubiquitin, TFIIA, guanine nucleotide-binding protein (beta-subunit), annexin I, a gene encoding a kinesin-like protein, and TWIST, which encodes a basic helix-loop-helix (bHLH) transcription factor implicated in Saethre-Chotzen syndrome (characterized by craniofacial and limb anomalies). Approximately 40% of these randomly analysed clones were full length. In addition to cDNAs matching known ESTs (Expressed Sequence Tags) in the GenBank and dbEST databases, novel sequences were detected at a frequency of 16% of randomly picked clones. The libraries are a valuable resource, providing longer cDNAs representing genes expressed during human preimplantation development.

摘要

我们描述了一种改进的高灵敏度方法,用于构建cDNA文库,该文库包含来自单个植入前人类胚胎和一个10周龄完整胎儿的、富含5'-编码序列的高比例cDNA。使用与磁珠相连的寡聚(dT)分离胚胎mRNA。第一链cDNA合成直接在结合的mRNA上进行,随后进行PCR,旨在扩增完整合成的cDNA分子。文库的复杂度在10⁵至10⁶个独立克隆之间。平均cDNA大小为1.0 kb,大小范围为0.5 - 3.0 kb。对胚胎文库中特定基因的PCR分析揭示了已知在植入前阶段转录的基因的转录本,如印记基因SNRPN、发育基因WNT11、HOX、OCT - 1和胚胎OCT - 4、细胞骨架基因角蛋白-18和β-肌动蛋白、细胞周期基因C - MOS以及管家基因GAPDH和HPRT。随机克隆的测序显示存在多种序列,如人绒毛膜促性腺激素、泛素、TFIIA、鸟嘌呤核苷酸结合蛋白(β亚基)、膜联蛋白I、一个编码驱动蛋白样蛋白的基因以及TWIST,后者编码一种与塞特勒-乔岑综合征(以颅面和肢体异常为特征)相关的碱性螺旋-环-螺旋(bHLH)转录因子。这些随机分析的克隆中约40%为全长。除了与GenBank和dbEST数据库中已知EST(表达序列标签)匹配的cDNA外,还以随机挑选克隆的16%的频率检测到新序列。这些文库是一种宝贵的资源,提供了代表人类植入前发育过程中表达基因的更长cDNA。

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