Study on the Imprinting Status of Insulin-Like Growth Factor II (IGF-II) Gene in Villus during 6–10 Gestational Weeks

Objective. To compare the difference of imprinting status of insulin-like growth factor II (IGF-II) gene in villus between normal embryo development group and abnormal embryo development group and to investigate the relationship between karyotype and the imprinting status of IGF-II gene. Methods. A...

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Main Authors: Jianhong Chen, Qun Fang, Baojiang Chen, Yi Zhou, Yanmin Luo
Format: Article
Language:English
Published: Wiley 2010-01-01
Series:Obstetrics and Gynecology International
Online Access:http://dx.doi.org/10.1155/2010/965905
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author Jianhong Chen
Qun Fang
Baojiang Chen
Yi Zhou
Yanmin Luo
author_facet Jianhong Chen
Qun Fang
Baojiang Chen
Yi Zhou
Yanmin Luo
author_sort Jianhong Chen
collection DOAJ
description Objective. To compare the difference of imprinting status of insulin-like growth factor II (IGF-II) gene in villus between normal embryo development group and abnormal embryo development group and to investigate the relationship between karyotype and the imprinting status of IGF-II gene. Methods. A total of 85 pregnant women with singleton pregnancy were divided into two groups: one with abnormal embryo development (n=38) and the other with normal embryo development (n=47). Apa I polymorphism of IGF-II gene in chorionic villus was assayed with reverse transcriptase polymerase chain reaction (RT-PCR) and restriction fragment length polymorphism (RFLP). The relationship between chromosomal abnormal karyotype and IGF-II gene imprinting status was analyzed by primary cell culture and G-banding chromosomal karyotype analysis. Results. IGF-II imprinting loss rate was higher in the abnormal embryo development group than the normal embryo development group (44.7% versus 31.6%), but without significant difference (P>.05). The percentage of abnormal chromosomes of chorionic villus in the abnormal embryo development group was 42.5%, in which IGF-II imprinting loss rate reached 64.7%. No abnormal karyotypes were found in the normal embryo development group. However, there was significant difference in IGF-II imprinting loss rate between two groups (P>.05). Conclusion. During weeks 6–10 of gestation, abnormal embryonic development is correlated with chromosomal abnormalities. The imprinting status of IGF-II gene played important roles in embryonic development, and imprinting loss might be related to chromosomal abnormalities.
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spelling doaj-art-650454efe7c540dab6bd0d740285c9972025-02-03T05:44:14ZengWileyObstetrics and Gynecology International1687-95891687-95972010-01-01201010.1155/2010/965905965905Study on the Imprinting Status of Insulin-Like Growth Factor II (IGF-II) Gene in Villus during 6–10 Gestational WeeksJianhong Chen0Qun Fang1Baojiang Chen2Yi Zhou3Yanmin Luo4Department of Obstetrics and Gynecology, Fetal Medical Center, First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510275, ChinaDepartment of Obstetrics and Gynecology, Fetal Medical Center, First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510275, ChinaDepartment of Obstetrics and Gynecology, Fetal Medical Center, First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510275, ChinaDepartment of Obstetrics and Gynecology, Fetal Medical Center, First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510275, ChinaDepartment of Obstetrics and Gynecology, Fetal Medical Center, First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510275, ChinaObjective. To compare the difference of imprinting status of insulin-like growth factor II (IGF-II) gene in villus between normal embryo development group and abnormal embryo development group and to investigate the relationship between karyotype and the imprinting status of IGF-II gene. Methods. A total of 85 pregnant women with singleton pregnancy were divided into two groups: one with abnormal embryo development (n=38) and the other with normal embryo development (n=47). Apa I polymorphism of IGF-II gene in chorionic villus was assayed with reverse transcriptase polymerase chain reaction (RT-PCR) and restriction fragment length polymorphism (RFLP). The relationship between chromosomal abnormal karyotype and IGF-II gene imprinting status was analyzed by primary cell culture and G-banding chromosomal karyotype analysis. Results. IGF-II imprinting loss rate was higher in the abnormal embryo development group than the normal embryo development group (44.7% versus 31.6%), but without significant difference (P>.05). The percentage of abnormal chromosomes of chorionic villus in the abnormal embryo development group was 42.5%, in which IGF-II imprinting loss rate reached 64.7%. No abnormal karyotypes were found in the normal embryo development group. However, there was significant difference in IGF-II imprinting loss rate between two groups (P>.05). Conclusion. During weeks 6–10 of gestation, abnormal embryonic development is correlated with chromosomal abnormalities. The imprinting status of IGF-II gene played important roles in embryonic development, and imprinting loss might be related to chromosomal abnormalities.http://dx.doi.org/10.1155/2010/965905
spellingShingle Jianhong Chen
Qun Fang
Baojiang Chen
Yi Zhou
Yanmin Luo
Study on the Imprinting Status of Insulin-Like Growth Factor II (IGF-II) Gene in Villus during 6–10 Gestational Weeks
Obstetrics and Gynecology International
title Study on the Imprinting Status of Insulin-Like Growth Factor II (IGF-II) Gene in Villus during 6–10 Gestational Weeks
title_full Study on the Imprinting Status of Insulin-Like Growth Factor II (IGF-II) Gene in Villus during 6–10 Gestational Weeks
title_fullStr Study on the Imprinting Status of Insulin-Like Growth Factor II (IGF-II) Gene in Villus during 6–10 Gestational Weeks
title_full_unstemmed Study on the Imprinting Status of Insulin-Like Growth Factor II (IGF-II) Gene in Villus during 6–10 Gestational Weeks
title_short Study on the Imprinting Status of Insulin-Like Growth Factor II (IGF-II) Gene in Villus during 6–10 Gestational Weeks
title_sort study on the imprinting status of insulin like growth factor ii igf ii gene in villus during 6 10 gestational weeks
url http://dx.doi.org/10.1155/2010/965905
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