The Molecular Basis for Hereditary Porcine Membranoproliferative Glomerulonephritis Type II
| Autor: | K. Høgåsen, T. Manuelian, Peter F. Zipfel, Guido Hegasy, Johan H. Jansen |
|---|---|
| Rok vydání: | 2002 |
| Předmět: |
chemistry.chemical_classification
medicine.medical_specialty medicine.diagnostic_test Point mutation Biology medicine.disease Molecular biology Pathology and Forensic Medicine Amino acid Secretory protein Endocrinology chemistry Western blot Internal medicine medicine Dense Deposit Disease Coding region Mesangial proliferative glomerulonephritis Nucleotide |
| Zdroj: | The American Journal of Pathology. 161:2027-2034 |
| ISSN: | 0002-9440 |
| Popis: | Porcine membranoproliferative glomerulonephritis type II in piglets of the Norwegian Yorkshire breed is considered the first animal model of human dense deposit disease. Porcine dense deposit disease is caused by the absence of the complement regulator factor H in plasma. Here we report the molecular basis for this absence. Single nucleotide exchanges at position C1590G and T3610G in the coding region of the factor H gene result in amino acid exchanges at nonframework residues L493V and I1166R that are located within SCR 9 and SCR 20, respectively. Apparently the L493V mutation represents a polymorphism whereas the I1166R causes the physiological consequences a block in protein secretion. Expression analysis shows comparable mRNA levels for factor H in liver tissue derived from both affected and healthy animals. In affected piglets, factor H protein is detected in increased amounts in liver cells. Factor H accumulates inside the hepatocytes and is not released as shown by Western blot analysis and immunohistochemistry. These data demonstrate that single amino acid exchanges of two nonframework amino acids either alone or in combination block protein secretion of factor H. This observation is also of interest for other human diseases in which factor H is involved, such as human factor H-associated form of hemolytic uremic syndrome. |
| Databáze: | OpenAIRE |
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