Myostatin belongs to the transforming growth factor‐β superfamily, and is expressed specifically in developing and mature skeletal muscle. Myostatin appears to act as a negative regulator of muscle development, since mice with targeted disruption of this gene display a large increase in muscle mass.
Linkage and physical mapping of prolactin to porcine chromosome 7
✍ Scribed by A. Vincent; L. Wang; C. K. Tuggle; M. F. Rothschild
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 227 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0268-9146
No coin nor oath required. For personal study only.
✦ Synopsis
Comparative mapping studies between human and pig have shown that there is conserved synteny between human chromosome 6 and pig chromosomes 1 and 7, but some gene locations are not well established. Prolactin (PRL), an anterior pituitary hormone, has been mapped to human chromosome 6, and has tentatively mapped to pig chromosome 7 using Southern‐RFLP analysis with a limited number of meioses. To confirm the assignment of prolactin to porcine chromosome 7 by physical and linkage analysis, pig cDNA and human genomic DNA sequences were used to design pig‐specific PCR primers. The primers amplified a fragment of ≈2·8 kb. Two polymorphic restriction sites were identified within this fragment with the restriction endonuclease __Bst__UI. Prolactin was significantly linked to six markers on the published PiGMaP map of pig chromosome 7. Prolactin was physically mapped using a pig × rodent somatic cell hybrid panel. An analysis of these data placed PRL on pig 7p1·1–p1·2 with 100% concordance and was in complete agreement with the linkage data. Both mapping techniques placed PRL in a conserved order with the loci in the syntenic region of human chromosome 6.
📜 SIMILAR VOLUMES
Swine chromosome 18 (SSC18) has the poorest marker density in the USDA‐MARC porcine linkage map. In order to increase the marker density, seven genes from human chromosome 7 (HSA7) expected to map to SSC18 were selected for marker development. The genes selected were: growth hormone releasing hormon