RECORD NO.: 95172532
AUTHOR: Ekstrom TJ
ADDRESS: Department of Clinical Neuroscience, Karolinska Hospital,
Stockholm, Sweden.
TITLE: Parental imprinting and the IGF2 gene.
SOURCE: Horm Res (GBI), 1994; 42 (4-5): 176-81
LANGUAGE: English
COUNTRY PUB.: SWITZERLAND
ANNOUNCEMENT: 9506
PUB. TYPE: JOURNAL ARTICLE; REVIEW; REVIEW, TUTORIAL
NUMBER REFS.: 38
ABSTRACT: The phenomenon of parental imprinting has become
increasingly important in disciplines such as evolution,
genetics, molecular biology, embryology and pathology.
Principally, parental imprinting refers to a parent-of-
origin dependent expression of a subset of autosomal loci,
independent of the sex of the offspring. Today, at least
seven such loci have been identified, including the human
IGF2 gene. It appears that the set of imprinted genes is not
always identical between the species, although the
importance of maintaining this kind of gene regulation is
evolutionarily conserved. It is particularly interesting
from the clinical point of view that a number of human
diseases, such as the Beckwith-Wiedemann and Prader-
Willi/Angelman syndromes, appear to involve unbalanced
parental contributions of imprinted loci. We show here that
the four different human IGF2 promoters are expressed mono-
and/or biallelically in complex patterns in postnatal liver
specimens.
MESH HEADINGS: *Genomic Imprinting; Insulin-Like Growth Factor II--genetics
(*GE); Fetal Development--genetics (GE); Genes, Suppressor,
Tumor; Liver--metabolism (ME); Mice; Models, Genetic;
Promoter Regions (Genetics); Animal; Female; Human; Male;
Support, Non-U.S. Gov't
GENE SYMBOL: IGF2; H19
CHEMICAL SUBS: 67763-97-7 (Insulin-Like Growth Factor II)
STANDARD NO.: 0301-0163
DATES: Entered 950330