Abstract
We have adopted a polymerase chain reaction approach to identify and clone a cDNA that contains the complete coding sequence of a novel fatty acid binding protein (FABP) from a rat brain λgt10 library. Sequencing of the brain FABP (B-FABP) cDNA revealed an open reading frame coding for a protein with 132 amino acids and a predicted size of ~15,000 Da. This putative protein shares extensive sequence homology with other members of the FABP family. Northern blot analysis using the B-FABP cDNA as a probe established the presence of an abundant mRNA ~0.8 kb long in rat brain and in the MOCH- 1 oligodendrocyte cell line. This transcript was also present in rat liver but not in other tissues examined. A developmental profile of this mRNA in rat brain demonstrated detectable expression in 15-day-old embryos with levels peaking in 1-day postnatal neonates and declining thereafter, reaching a low steady-state level at 3 weeks of age. In situ hybridization histochemistry revealed B-FABP mRNA in various brain regions, with the highest levels in fiber tracts. The B-FABP message was also detected at a lower level in several gray matter regions. The cloning approach used in this study would likely be useful in the identification and isolation of FABP- encoding genes from other tissues and species.
Original language | English (US) |
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Pages (from-to) | 1616-1624 |
Number of pages | 9 |
Journal | Journal of neurochemistry |
Volume | 63 |
Issue number | 5 |
DOIs | |
State | Published - Nov 1994 |
Funding
Keywords
- Cloning
- Development
- Fatty acid binding protein
- In situ hybridization
- MOCH-1 cells
- Myelin
- cDNA
ASJC Scopus subject areas
- Cellular and Molecular Neuroscience
- Biochemistry