Your browser doesn't support javascript.
loading
Physical linkage of the A-raf-1, properdin, synapsin I, and TIMP genes on the human and mouse X chromosomes.
Derry, J M; Barnard, P J.
Affiliation
  • Derry JM; MRC Molecular Neurobiology Unit, MRC Centre, Cambridge, United Kingdom.
Genomics ; 12(4): 632-8, 1992 Apr.
Article in En | MEDLINE | ID: mdl-1572636
ABSTRACT
Genes encoding the neuron-specific phosphoprotein synapsin I (SYN1), the glycoprotein tissue inhibitor of metalloproteinases (TIMP), the proto-oncogene A-raf-1 (ARAF1), and properdin (PFC), a positive regulator of the alternative pathway of human complement, lie within a conserved synteny encompassing the proximal short arm of the human X chromosome (Xp21.1-p11) and the centromeric end of the mouse X chromosome (A1-A5). We have used a mouse interspecific cross to demonstrate genetic linkage of Syn-1, Timp, and Araf and also show physical linkage, with Timp lying only 10 kb from Araf, within an intron of the Syn-1 gene. Detailed restriction mapping shows that Timp is transcribed in the same direction as Araf but in the opposite direction to the Syn-1 gene. Analysis of the corresponding region of the human X chromosome indicates a similar arrangement and in addition shows that the properdin gene lies within 5 kb of the 5' end of the synapsin I gene.
Subject(s)
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Synapsins Limits: Animals / Humans Language: En Journal: Genomics Journal subject: GENETICA Year: 1992 Document type: Article Affiliation country: United kingdom
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Synapsins Limits: Animals / Humans Language: En Journal: Genomics Journal subject: GENETICA Year: 1992 Document type: Article Affiliation country: United kingdom