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Expression of exon 3-retaining and exon 3-excluding isoforms of the human growth hormone-receptor is regulated in an interindividual, rather than a tissue-specific, manner.
- Source :
-
The Journal of clinical endocrinology and metabolism [J Clin Endocrinol Metab] 1995 Jul; Vol. 80 (7), pp. 2154-7. - Publication Year :
- 1995
-
Abstract
- GH has multiple effects on growth and metabolism, and these functions are mediated through binding to specific cell surface receptors. The human GH receptor (GHR) exists in two known isoforms; in one form exon 3 is present (GHR3+), and in the other, exon 3 is absent (GHR3-). Recent reports have suggested that the expression of the two isoforms is tissue specific and/or developmentally regulated. We used a reverse transcription-polymerase chain reaction assay to study the expression pattern of the two isoforms in a variety of tissues from normal subjects and patients with acromegaly. In skeletal muscle from both normal subjects and patients with acromegaly, the GHR3+ transcript was expressed, either alone or together with the shorter (GHR3-) transcript. When multiple tissues from six subjects were tested, the expression of the two isoforms varied among subjects, whereas different tissues from the same subject showed the same expression pattern. These results indicate that the expression of the GHR isoforms is not tissue specific. Instead, the expression of the GHR isoforms appears to be specific for each individual, suggesting that it is under the control of factors that affect all tissues in the body.
- Subjects :
- Adipose Tissue metabolism
Adolescent
Adult
Aged
Aged, 80 and over
Base Sequence
Bone and Bones metabolism
Cartilage metabolism
Child
Child, Preschool
DNA Primers
Female
Humans
Infant
Liver metabolism
Male
Middle Aged
Molecular Sequence Data
Muscle, Skeletal metabolism
Organ Specificity
Polymerase Chain Reaction
Skin metabolism
Exons
Gene Expression Regulation
Receptors, Somatotropin biosynthesis
Receptors, Somatotropin genetics
Subjects
Details
- Language :
- English
- ISSN :
- 0021-972X
- Volume :
- 80
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- The Journal of clinical endocrinology and metabolism
- Publication Type :
- Academic Journal
- Accession number :
- 7608270
- Full Text :
- https://doi.org/10.1210/jcem.80.7.7608270