Next Article in Journal / Special Issue
Biochemical Analyses of Csx/Nkx2.5 Mutants and Their Structure–Function Relationship
Previous Article in Journal
The SPASIBA Force Field for Studying Iron-Tannins Interactions : Application to Fe3+ /Fe2+ Catechol Complexe
Previous Article in Special Issue
Effects of Acetazolamide Combined with or without NaHCO3 on Suppressing Neoplasm Growth, Metastasis and Aquaporin-1 (AQP1) Protein Expression
Int. J. Mol. Sci. 2007, 8(4), 273-283; doi:10.3390/i8040273

Imprinting Status of IGF2 in Cord Blood Cells of Han Chinese Newborns

1, 1, 1, 2, 2, 1, 1, 1, 3, 1,*  and 4,*
Received: 13 December 2006 / Accepted: 23 March 2007 / Published: 15 April 2007
(This article belongs to the Special Issue Interaction of Biological Molecules)
View Full-Text   |   Download PDF [80 KB, uploaded 19 June 2014]   |   Browse Figure
Abstract: Loss of imprinting (LOI) of insulin-like growth factor II gene (IGF2) is anepigenetic abnormality associated with human diseases. However, little is known about thecharacteristics of IGF2 imprinting in newborn cord blood cells. METHODS: A total of 923cord blood samples from term singletons and related clinical data were collected; IGF2imprinting status in 273 specimens were successfully analyzed using RT-PCR andrestriction fragment length polymorphism. RESULTS: LOI of IGF2 was detected in 20.9%of informative samples. The mean birth weights (BW) in the LOI and the normal imprintinggroups were 3462.7 ± 460.2 g and 3363.7 ± 427.7 g, respectively. The abdominal perimetersin the LOI group tended to be larger than that in the normal imprinting group. Pregnancycomplications, delivery modes, newborn diseases, occurrences of malignant tumors ingrandparents, and other maternal factors were not associated with LOI of IGF2. 22.2% ofthe infants with IGF2 LOI also showed LOI in their father’s lymphocytes while 21.4% intheir mother’s lymphocytes. CONCLUSIONS: About 20% of Han Chinese newbornsindicated LOI of IGF2 in their cord blood lymphocytes that may represent the epigeneticcharacteristics in this ethnic group. While IGF2 LOI tends to be weakly inherited between parents and offspring, abnormal imprinting seems to be statistically unrelated with phenotypes of newborns, although it might have an association with later phenotypes of infants.
Keywords: IGF2; genomic imprinting; cord blood; birth weight; Han Chinese IGF2; genomic imprinting; cord blood; birth weight; Han Chinese
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Export to BibTeX |

MDPI and ACS Style

Dai, Y.; Wang, Z.; Li, J.; Gu, X.; Zheng, M.; Zhou, J.; Ye, X.; Yao, J.; Cui, I.; Hu, Y.; Cui, H. Imprinting Status of IGF2 in Cord Blood Cells of Han Chinese Newborns. Int. J. Mol. Sci. 2007, 8, 273-283.

AMA Style

Dai Y, Wang Z, Li J, Gu X, Zheng M, Zhou J, Ye X, Yao J, Cui I, Hu Y, Cui H. Imprinting Status of IGF2 in Cord Blood Cells of Han Chinese Newborns. International Journal of Molecular Sciences. 2007; 8(4):273-283.

Chicago/Turabian Style

Dai, Yimin; Wang, Zhiqun; Li, Jie; Gu, Xiangfang; Zheng, Mingming; Zhou, Jianjun; Ye, Xiaodong; Yao, Jincui; Cui, Isabelle; Hu, Yali; Cui, Hengmi. 2007. "Imprinting Status of IGF2 in Cord Blood Cells of Han Chinese Newborns." Int. J. Mol. Sci. 8, no. 4: 273-283.

Int. J. Mol. Sci. EISSN 1422-0067 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert