Hamel Melanie, Dufort Isabelle, Robert Claude, Gravel Catherine, Leveille Marie-Claude, Leader Arthur, Sirard Marc-Andre
Département des Sciences Animales, Centre de Recherche en Biologie de la Reproduction, Université Laval, Québec, Canada G1K 7P4.
Hum Reprod. 2008 May;23(5):1118-27. doi: 10.1093/humrep/den048. Epub 2008 Feb 28.
The development of an accurate method for selection of high-quality embryos is essential to achieve high pregnancy rates with single embryo transfer in human IVF. The developmental competence of the oocyte is acquired during follicle maturation and strong communication also exists between the follicular cells (FCs) and the oocytes; thus oocyte developmental competence may be determined by markers expressed in the surrounding FCs.
From consenting patients (n = 40), FCs were recovered on a per follicle basis by individual follicle puncture. Hybridization analyses using a custom-made complementary DNA microarray containing granulosa/cumulus expressed sequence tags (ESTs) from subtracted libraries and an Affymetrix GeneChip were performed to identify specific genes expressed in follicles leading to a pregnancy. The selected candidate genes were validated by quantitative-PCR (Q-PCR).
Subtractive libraries prepared from pooled samples representing pregnant versus non-pregnant patients produced 1694 ESTs. Hybridization data analysis discriminated 115 genes associated with competent follicles. Selected candidates were confirmed by Q-PCR: 3-beta-hydroxysteroid dehydrogenase 1 (P = 0.0078), Ferredoxin 1 (P = 0.0203), Serine (or cysteine) proteinase inhibitor clade E member 2 (P = 0.0499), Cytochrome P450 aromatase (P = 0.0359) and Cell division cycle 42 (P = 0.0396).
Microarray technologies are useful to mine the transcriptome of FCs expressed in follicles associated with competent oocytes and could be used to improve embryo selection with the objective of successful single embryo transfer.
开发一种准确选择高质量胚胎的方法对于人类体外受精(IVF)中通过单胚胎移植实现高妊娠率至关重要。卵母细胞的发育能力在卵泡成熟过程中获得,并且卵泡细胞(FCs)与卵母细胞之间也存在密切的交流;因此,卵母细胞的发育能力可能由周围卵泡细胞中表达的标志物决定。
从40名同意参与的患者中,通过单个卵泡穿刺逐个回收卵泡细胞。使用定制的包含来自消减文库的颗粒细胞/卵丘表达序列标签(ESTs)的互补DNA微阵列和Affymetrix基因芯片进行杂交分析,以鉴定在导致妊娠的卵泡中表达的特定基因。所选的候选基因通过定量PCR(Q-PCR)进行验证。
从代表妊娠与未妊娠患者的混合样本中制备的消减文库产生了1694个ESTs。杂交数据分析区分出115个与有发育能力卵泡相关的基因。所选候选基因通过Q-PCR得到确认:3-β-羟基类固醇脱氢酶1(P = 0.0078)、铁氧化还原蛋白1(P = 0.0203)、丝氨酸(或半胱氨酸)蛋白酶抑制剂E家族成员2(P = 0.0499)、细胞色素P450芳香化酶(P = 0.0359)和细胞分裂周期42(P = 0.0396)。
微阵列技术有助于挖掘与有发育能力卵母细胞相关的卵泡中表达的卵泡细胞转录组,并可用于改进胚胎选择,以实现单胚胎移植成功的目标。