Systems analysis of matrix metalloproteinase mRNA expression in skeletal tissues

Front Biosci. 2002 Jun 1:7:a126-34. doi: 10.2741/qian.

Abstract

The availability of human genome sequences provides life scientists and biomedical engineers with a challenging opportunity to develop computational and experimental tools for quantitatively analyzing biological processes. In response to a growing need to integrate experimental mRNA expression data with human genome sequences, we present here a unique analysis named "Promoter-Based Estimation (PROBE)" analysis. The PROBE analysis is "systems analysis" of transcriptional processes using control and estimation theories. A linear model was built in order to estimate the mRNA levels of a group of genes from their regulatory DNA sequences. The model was also used to interpret two independent datasets in skeletal tissues. The results demonstrated that the mRNA levels of a family of matrix metalloproteinases can be modeled from a distribution of cis-acting elements on regulatory DNA sequences. The model accurately predicted a stimulatory role of cis-acting elements such as AP1, NFY, PEA3, and Sp1 as well as an inhibitory role of AP2. These predictions are consistent with biological observations, and a specific assay for testing such predictions is proposed. Although eukaryotic transcription is a complex mechanism, the two examples presented here support the potential use of the described analysis for elucidating the functional significance of DNA regulatory elements.

Publication types

  • Research Support, Non-U.S. Gov't
  • Validation Study

MeSH terms

  • Algorithms
  • Bone and Bones / enzymology*
  • Computational Biology / methods*
  • Computational Biology / statistics & numerical data
  • Databases, Genetic
  • Enzyme Induction / genetics
  • Enzyme Repression / genetics
  • Genes, Regulator / genetics
  • Genetic Variation / genetics
  • Genome, Human
  • Humans
  • Linear Models
  • Matrix Metalloproteinases / biosynthesis*
  • Matrix Metalloproteinases / genetics
  • Models, Genetic
  • RNA, Messenger / biosynthesis*
  • Sensitivity and Specificity
  • Transcription, Genetic / genetics

Substances

  • RNA, Messenger
  • Matrix Metalloproteinases