Hypotensive effect associated with a phospholipase C-delta 1 gene mutation in the spontaneously hypertensive rat

Biochem Biophys Res Commun. 1992 Sep 30;187(3):1359-66. doi: 10.1016/0006-291x(92)90452-q.

Abstract

To identify the genes responsible for blood pressure in the spontaneously hypertensive rat strain, we performed a cosegregation analysis between the genotype and blood pressure in a set of male F2 rats obtained by crossmating SHR with Wistar-Kyoto rats, a parental normotensive strain. Our investigation revealed that the phospholipase C-delta 1 polymorphism, which resulted in missense mutation, cosegregates with the lower blood pressure in SHR, and that PLC-delta 1 gene is located on chromosome 8. On the other hand, we found the lack of cosegregation between blood pressure and the nerve growth factor receptor gene, which is linked to a hypertensinogenic gene locus (denoted as BP/SP-1) on chromosome 10. We propose that PLC-delta 1 gene itself of closely linked gene on chromosome 8 is a new candidate with the hypotensive effect, and that BP-SP1 locus does not directly contribute to blood pressure elevation in original SHR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Blood Pressure
  • Chromosome Mapping
  • Hypertension / genetics*
  • Male
  • Molecular Sequence Data
  • Mutation
  • Oligodeoxyribonucleotides / chemistry
  • Polymerase Chain Reaction
  • Polymorphism, Restriction Fragment Length
  • Rats
  • Rats, Inbred SHR / genetics*
  • Rats, Inbred WKY / genetics
  • Receptors, Nerve Growth Factor / genetics
  • Type C Phospholipases / genetics*

Substances

  • Oligodeoxyribonucleotides
  • Receptors, Nerve Growth Factor
  • Type C Phospholipases