New insights into growth hormone action
It has been 75 years since Evans and Long identified a somatic growth-promoting substance in pituitary extracts, yet it is only in the last 20 years that the molecular basis for this action has been established. Three key elements in this elucidation were the cloning of the GH receptor, the identifi...
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| Vydané v: | Journal of molecular endocrinology Ročník 36; číslo 1; s. 1 |
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| Hlavní autori: | , , , , |
| Médium: | Journal Article |
| Jazyk: | English |
| Vydavateľské údaje: |
England
01.02.2006
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| ISSN: | 0952-5041 |
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| Abstract | It has been 75 years since Evans and Long identified a somatic growth-promoting substance in pituitary extracts, yet it is only in the last 20 years that the molecular basis for this action has been established. Three key elements in this elucidation were the cloning of the GH receptor, the identification of Janus kinase (JAK) 2 as the receptor-associated tyrosine kinase, and the delineation of signal transduction and activators of transcription (STAT) 5a/b as the key transcription factor(s) activated by JAK2. The interaction between these three elements results in enhanced postnatal growth and is the subject of this review. We describe a new model for GH receptor activation based on subunit rotation within a constitutive dimer, together with the phenotype and hepatic transcript profile of mice with targeted knockins to the receptor cytoplasmic domain. These support a central role for STAT5a/b in postnatal growth. |
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| AbstractList | It has been 75 years since Evans and Long identified a somatic growth-promoting substance in pituitary extracts, yet it is only in the last 20 years that the molecular basis for this action has been established. Three key elements in this elucidation were the cloning of the GH receptor, the identification of Janus kinase (JAK) 2 as the receptor-associated tyrosine kinase, and the delineation of signal transduction and activators of transcription (STAT) 5a/b as the key transcription factor(s) activated by JAK2. The interaction between these three elements results in enhanced postnatal growth and is the subject of this review. We describe a new model for GH receptor activation based on subunit rotation within a constitutive dimer, together with the phenotype and hepatic transcript profile of mice with targeted knockins to the receptor cytoplasmic domain. These support a central role for STAT5a/b in postnatal growth.It has been 75 years since Evans and Long identified a somatic growth-promoting substance in pituitary extracts, yet it is only in the last 20 years that the molecular basis for this action has been established. Three key elements in this elucidation were the cloning of the GH receptor, the identification of Janus kinase (JAK) 2 as the receptor-associated tyrosine kinase, and the delineation of signal transduction and activators of transcription (STAT) 5a/b as the key transcription factor(s) activated by JAK2. The interaction between these three elements results in enhanced postnatal growth and is the subject of this review. We describe a new model for GH receptor activation based on subunit rotation within a constitutive dimer, together with the phenotype and hepatic transcript profile of mice with targeted knockins to the receptor cytoplasmic domain. These support a central role for STAT5a/b in postnatal growth. It has been 75 years since Evans and Long identified a somatic growth-promoting substance in pituitary extracts, yet it is only in the last 20 years that the molecular basis for this action has been established. Three key elements in this elucidation were the cloning of the GH receptor, the identification of Janus kinase (JAK) 2 as the receptor-associated tyrosine kinase, and the delineation of signal transduction and activators of transcription (STAT) 5a/b as the key transcription factor(s) activated by JAK2. The interaction between these three elements results in enhanced postnatal growth and is the subject of this review. We describe a new model for GH receptor activation based on subunit rotation within a constitutive dimer, together with the phenotype and hepatic transcript profile of mice with targeted knockins to the receptor cytoplasmic domain. These support a central role for STAT5a/b in postnatal growth. |
| Author | Waters, M J Fairlie, D P Pelekanos, R A Brown, R J Hoang, H N |
| Author_xml | – sequence: 1 givenname: M J surname: Waters fullname: Waters, M J email: m.waters@imb.uq.edu.au organization: Institute for Molecular Bioscience and School of Biomedical Sciences, University of Queensland, St Lucia, Australia 4072. m.waters@imb.uq.edu.au – sequence: 2 givenname: H N surname: Hoang fullname: Hoang, H N – sequence: 3 givenname: D P surname: Fairlie fullname: Fairlie, D P – sequence: 4 givenname: R A surname: Pelekanos fullname: Pelekanos, R A – sequence: 5 givenname: R J surname: Brown fullname: Brown, R J |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/16461922$$D View this record in MEDLINE/PubMed |
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| SubjectTerms | Amino Acid Sequence Animals Cloning, Molecular Growth Hormone - genetics Growth Hormone - metabolism Growth Hormone - physiology Humans Janus Kinase 2 Mice Models, Molecular Molecular Sequence Data Protein Conformation Protein-Tyrosine Kinases - chemistry Protein-Tyrosine Kinases - metabolism Proto-Oncogene Proteins - chemistry Proto-Oncogene Proteins - metabolism STAT5 Transcription Factor - physiology STAT6 Transcription Factor - physiology |
| Title | New insights into growth hormone action |
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