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Silver-Russell综合征的分子与临床发现及其相关性:IGF2在生长决定中的积极作用以及IGF2-H19结构域在身体和胎盘中的差异印记调控的意义

Molecular and clinical findings and their correlations in Silver-Russell syndrome: implications for a positive role of IGF2 in growth determination and differential imprinting regulation of the IGF2-H19 domain in bodies and placentas.

作者信息

Yamazawa Kazuki, Kagami Masayo, Nagai Toshiro, Kondoh Tatsuro, Onigata Kazumichi, Maeyama Katsuhiro, Hasegawa Tomonobu, Hasegawa Yukihiro, Yamazaki Toshio, Mizuno Seiji, Miyoshi Yoko, Miyagawa Shinichiro, Horikawa Reiko, Matsuoka Kentaro, Ogata Tsutomu

机构信息

Department of Endocrinology and Metabolism, National Research Institute for Child Health and Development, Tokyo, Japan.

出版信息

J Mol Med (Berl). 2008 Oct;86(10):1171-81. doi: 10.1007/s00109-008-0377-4. Epub 2008 Jul 8.

Abstract

Silver-Russell syndrome (SRS) is characterized by growth failure and dysmorphic features and is frequently caused by hypomethylation (epimutation) of the H19-DMR. Although molecular and clinical studies have extensively been performed for SRS patients themselves, such studies have not been carried out for placentas. We identified 20 epimutation-positive and 40 epimutation-negative Japanese SRS patients and obtained placental weight data from 12 epimutation-positive and ten epimutation-negative patients and paraffin-embedded placental tissues for molecular and histological examinations from three epimutation-positive and two epimutation-negative patients. Methylation patterns were comparable between leukocytes and placentas in both epimutation-positive and epimutation-negative patients. Epimutations resulted in virtually no IGF2 expression and biallelic slight H19 expression in the leukocytes and obviously reduced IGF2 expression of paternal origin and nearly normal H19 expression of maternal origin in the placentas. Epimutation-positive patients had characteristic body phenotype and small placentas with hypoplastic chorionic villi, and epimutation-negative patients had somewhat small placentas with hypoplastic chorionic villi or massive infarction. Furthermore, significant correlations were identified between the H19-DMR methylation index and the body and placental sizes and between the placental weight and the body size in the epimutation-positive patients, whereas such correlations were not detected for the head circumference. These results suggest (1) characteristic phenotype and reduced IGF2 expression in the epimutation-positive placentas; (2) similarities and differences in the epigenetic control of the IGF2-H19 domain between leukocytes and placentas; (3) a positive role of the IGF2 expression level, as reflected by the methylation index, in the determination of body and placental growth in epimutation-positive patients, except for the brain where IGF2 is expressed biallelically; (4) involvement of placental dysfunction in prenatal growth failure; and (5) relevance of both (epi)genetic factor(s) and environmental factor(s) to SRS in epimutation-negative patients.

摘要

Silver-Russell综合征(SRS)的特征为生长发育迟缓及畸形特征,常由H19基因差异甲基化区域(H19-DMR)的低甲基化(表观突变)引起。尽管针对SRS患者自身已广泛开展了分子和临床研究,但尚未对胎盘进行此类研究。我们鉴定出20例表观突变阳性和40例表观突变阴性的日本SRS患者,获取了12例表观突变阳性和10例表观突变阴性患者的胎盘重量数据,并从3例表观突变阳性和2例表观突变阴性患者处获取了石蜡包埋的胎盘组织用于分子和组织学检查。表观突变阳性和表观突变阴性患者的白细胞与胎盘之间的甲基化模式具有可比性。表观突变导致白细胞中几乎无IGF2表达且H19呈双等位基因轻度表达,而胎盘中父源IGF2表达明显降低,母源H19表达近乎正常。表观突变阳性患者具有特征性的身体表型且胎盘小,伴有绒毛膜绒毛发育不全,表观突变阴性患者的胎盘稍小,伴有绒毛膜绒毛发育不全或大面积梗死。此外,在表观突变阳性患者中,H19-DMR甲基化指数与身体及胎盘大小之间以及胎盘重量与身体大小之间存在显著相关性,而头围未检测到此类相关性。这些结果表明:(1)表观突变阳性胎盘中具有特征性表型且IGF2表达降低;(2)白细胞与胎盘之间IGF2-HID区域表观遗传调控的异同;(3)甲基化指数所反映的IGF2表达水平在表观突变阳性患者身体和胎盘生长的决定中起积极作用,但大脑中IGF2呈双等位基因表达的情况除外;(4)胎盘功能障碍与产前生长发育迟缓有关;(5)表观突变阴性患者中(表观)遗传因素和环境因素均与SRS相关。

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