Insulin-like growth factor 2 (IGF-2) is one of three protein hormones that share structural similarity to insulin.
Gene structure
In humans, the IGF2
gene is located on
chromosome 11p15.5, a region which contains numerous
imprinted genes. In mice this
homologous region is found at
distal chromosome 7. In both organisms,
Igf2 is imprinted, with expression resulting favourably from the paternally inherited
allele.
The protein CTCF is involved in repressing expression of the gene, by binding to the H19 imprinting control region (ICR) along with Differentially-methylated Region-1 (DMR1) and Matrix Attachment Region -3 (MAR3). These three DNA sequences bind to CTCF in a way that limits downstream enhancer access to the Igf2 region. The mechanism in which CTCF binds to these regions is currently unknown, but could include either a direct DNA-CTCF interaction or it could possibly be mediated by other proteins
Protein structure
IGF-2 exerts its effects by binding to the
IGF-1 receptor. IGF2 may also bind to the
IGF-2 receptor (also called the cation-independent
mannose 6-phosphate receptor), which acts as a
signalling antagonist; that is, to prevent IGF2 responses.
Function
The major role of IGF2 is as a growth promoting hormone during
gestation.
Diseases
It is sometimes produced in non-islet cell
tumours, causing
hypoglycemia (
Doege-Potter syndrome).
See also
External links
References
Further reading