Table 3.

Detection of Clones With Identical Ig/c-mycHybrid Sequences in Different Regions of the Intestine

StrainPristane3-150Intestinal Distribution3-151
DuodenumJejunumIleumColon
BALB/cAn3-152 − − x − − − − − − x − 
BALB/cAn − − − − − − − − x x − 
BALB/cAn − − x − x − − − − 
BALB/cAn − − − − − − x − x − 
BALB/cAn − − − − − x x − − 
C3H/HeJ − − − − − − x x x − 
C3H/HeJ − − x x − − − − − − 
C57BL/6 − − − − − − x − − 
StrainPristane3-150Intestinal Distribution3-151
DuodenumJejunumIleumColon
BALB/cAn3-152 − − x − − − − − − x − 
BALB/cAn − − − − − − − − x x − 
BALB/cAn − − x − x − − − − 
BALB/cAn − − − − − − x − x − 
BALB/cAn − − − − − x x − − 
C3H/HeJ − − − − − − x x x − 
C3H/HeJ − − x x − − − − − − 
C57BL/6 − − − − − − x − − 

The PCR amplification of such a recombination is marked by a cross. Tissues that were negative for that particular clone could harbor cells with an unrelated Ig/c-myc sequence. Note that identical Ig/c-myc sequences were amplified from noncontiguous intestinal samples in several cases. Therefore, a cross-contamination during the dissection appears to be unlikely.

F3-150

Before (−) or 7 days after (+) the injection of pristane.

F3-151

DNA preparations were made from the entire duodenum, two pieces of the jejunum, six pieces of the ileum, and from the entire colon.

F3-152

Each line represents a single clone of cells with identical Ig/c-myc sequences that was detected in different intestinal DNA preparations.

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