AND THE QUESTION IS ? ? ?
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questions are sought from appropriate sources (i.e. physicians,
researchers, respiratory therapists, etc). Write to the editor
(editor@iacfa.org) with
your questions and queries and we will attempt to answer them
for you.
The 5T Mutation in the CFTR Gene
Dear Editor
I have just been diagnosed for being
positive for the 5T allele in intron 8. I am negative for
the main gene of CF, but the 5T allele is a mutation of some
sort in CF. How can this affect my children? What if my husband
has the same gene? What if he doesn't?
Natasha Trajkova
New Jersey, USA
Professor Dieter Gruenert, a Genetics advisor to IACFA
replies:
There is limited information correlating genetic anomalies
in the CFTR gene with specific phenotypic/pathological characteristics.
What is known about the 5T mutation, is that it causes abnormal
splicing of the messenger RNA (mRNA) (i.e., the way that the
pieces of the gene that give rise to the mRNA are put together)
and that there
appears to be lower levels of the CFTR mRNA expressed from
the chromosome carrying this particular mutation. If it occurs
without any other pathological mutations in the CFTR, in most
cases there does not appear to be any associated 5T-specific
pathology.
There have been reports of exceptions with regard to the
question of pathology that appear to be dependent on the overall
genetic background (i.e., not all genes are expressed in the
same way in all individuals thus giving rise to variations
in the genetic
background). There are scattered conflicting reports as to
the contribution of the 5T mutation to the lung function anomalies.
Overall, the consensus is that the 5T mutation alone is not
pathogenic, but if it is associated with CFTR pathogenic mutation,
there may be an associated pathology that could be manifested
in male infertility or mild lung function anomalies.
I hope that this helps answer some of your concerns.
GLOSSARY
Anomalies = Differences
mRNA = messengerRNA = The genetic information taken
from a gene responsible for the protein.
Pathological = Disease
Phenotypic = How genes are expressed in the individual
(e.g. you may have the genes for blue eyes, but still have
brown eyes or phenotype)
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