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The growth hormone receptor messenger ribonucleic acid present in ovine fetal liver is a variant form
1Department of Animal Sciences, University of Missouri, Columbia 65211, USA.
Abstract:
Specific binding of ovine GH (oGH) to microsomal membranes isolated from fetal sheep liver is slight to nonexistent. The complementary DNA sequence encoding the oGH receptor (oGHR) has been reported, and Northern blot analysis has indicated that oGHR messenger RNA (mRNA) is present in fetal liver and skeletal muscle from mid- to late gestation. In human tissues, the GHR mRNA exists in multiple forms, including the deletion of exon 3 and variable 5'-untranslated regions. In rodents, the GHR mRNA exists in two forms, one encoding the membrane-bound receptor and the other encoding the soluble GH-binding protein. To further characterize the oGHR mRNA transcript present in ovine fetal liver during gestation, we designed a series of primers to be used in reverse transcriptase-polymerase chain reactions (RT-PCR), which generate products that span from the 5'-untranslated region through the coding region of the oGHR mRNA. Nucleotide sequences of the resulting complementary DNAs revealed that an oGHR mRNA is present from mid- to late gestation (days 60-135) which contains the region analogous to exon 3 of the human GHR gene. However, the 5'-untranslated region previously reported in adult tissues was not present until day 135 of gestation in fetal liver, nor was it present in day 100 fetal skeletal muscle. Northern hybridization analysis indicates that the major oGHR transcript in day 105 fetal liver is 5.8 kilobases (kb) in size, with minor transcripts observed at 4.7 kb and three transcripts greater than 6.5 kb. By day 135 of gestation, the transcript size is the same as that observed in day 100 pregnant ewe liver (5.5 kb). We conclude that the oGHR mRNA present in midgestation fetal liver differs structurally from the transcript present in late gestation fetal liver and adult liver, and this difference may explain the lack of specific GH binding to ovine fetal liver membranes. Furthermore, our results suggest that there is a developmental switch in the structure of oGHR mRNA that occurs shortly before term, potentially preparing the fetus to respond to GH postnatally.
Insights
Ovine growth hormone (oGH) receptor messenger RNA (mRNA) in fetal sheep liver changes structure during gestation. This developmental switch in oGHR mRNA may explain low GH binding in fetal liver before birth.
Area of Science:
- Reproductive Endocrinology
- Developmental Biology
- Molecular Genetics
Background:
- Specific binding of ovine growth hormone (oGH) to fetal sheep liver is minimal.
- Ovine growth hormone receptor (oGHR) mRNA is present in fetal liver and muscle, but its structure during gestation is not fully characterized.
- Human and rodent GHR mRNA exist in multiple forms, suggesting similar complexity in sheep.
Purpose of the Study:
- To characterize the ovine growth hormone receptor (oGHR) mRNA transcript in ovine fetal liver throughout gestation.
- To investigate potential structural differences in oGHR mRNA that could explain the lack of GH binding in fetal liver.
Main Methods:
- Reverse transcriptase-polymerase chain reaction (RT-PCR) was used to amplify oGHR mRNA from fetal sheep liver and skeletal muscle.
- Nucleotide sequencing of RT-PCR products.
- Northern hybridization analysis of oGHR mRNA transcripts.
Main Results:
- Ovine GHR (oGHR) mRNA containing the exon 3 region analog was detected from mid- to late gestation (days 60-135).
- The 5'-untranslated region, present in adult oGHR mRNA, was absent in fetal liver until day 135 and in fetal muscle at day 100.
- Major oGHR transcript size in fetal liver changed from 5.8 kb at day 105 to 5.5 kb by day 135, matching adult ewe liver transcripts.
Conclusions:
- Ovine GHR mRNA structure differs between midgestation fetal liver and late gestation/adult liver.
- This structural variation in oGHR mRNA likely accounts for the low specific GH binding observed in ovine fetal liver membranes.
- A developmental switch in oGHR mRNA structure occurs before term, potentially enabling postnatal GH responsiveness.