Identification of differentially expressed genes in the kidneys of growth hormone transgenic mice

K. T. Coschigano, A. N. Wetzel, N. Obichere, A. Sharma, S. Lee, R. Rasch, M. M. Guigneaux, A. Flyvbjerg, T. G. Wood, J. J. Kopchick

Research output: Contribution to journalArticlepeer-review

12 Scopus citations


Objective: Bovine growth hormone (bGH) transgenic mice develop severe kidney damage. This damage may be due, at least in part, to changes in gene expression. Identification of genes with altered expression in the bGH kidney may identify mechanisms leading to damage in this system that may also be relevant to other models of kidney damage. Design: cDNA subtraction libraries, northern blot analyses, microarray analyses and real-time reverse transcription polymerase chain reaction (RT/PCR) assays were used to identify and verify specific genes exhibiting differential RNA expression between kidneys of bGH mice and their non-transgenic (NT) littermates. Results: Immunoglobulins were the vast majority of genes identified by the cDNA subtractions and the microarray analyses as being up-regulated in bGH. Several glycoprotein genes and inflammation-related genes also showed increased RNA expression in the bGH kidney. In contrast, only a few genes were identified as being significantly down-regulated in the bGH kidney. The most notable decrease in RNA expression was for the gene encoding kidney androgen-regulated protein. Conclusions: A number of genes were identified as being differentially expressed in the bGH kidney. Inclusion of two groups, immunoglobulins and inflammation-related genes, suggests a role of the immune system in bGH kidney damage.

Original languageEnglish (US)
Pages (from-to)345-355
Number of pages11
JournalGrowth Hormone and IGF Research
Issue number5
StatePublished - Oct 2010
Externally publishedYes


  • CDNA subtraction
  • Chemokine (C-C motif) ligand 2/monocyte chemotactic protein-1
  • Growth hormone transgenic mice
  • Immunoglobulins
  • Inflammation
  • Kidney
  • Kidney androgen-regulated protein
  • Microarray
  • Real-time RT/PCR

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Endocrinology


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