Jäckel M, Witt C, Antonova O, Curdt I, Labeit S, Jockusch H
Developmental Biology Unit, University of Bielefeld, Germany.
FEBS Lett. 1997 May 12;408(1):21-4. doi: 10.1016/s0014-5793(97)00381-5.
The gene for titin, a 4MDa myofibrillar protein, was analysed in golden hamster DNAs from different sources, using human cDNA probes and PCR. In the DNA from the BHK-21-Bi subline of baby hamster kidney cells, extended sequences coding for Z-line associated domains were missing, indicating a deletion that renders titin non-functional. These sequences were present in the original BHK-21 line and in hamster DNAs. Our finding shows that, due to the absence of selective pressure on a gene's function, genomic deterioration can occur in a permanent cell line and can lead to a loss of overlapping DNA stretches in both autosomes.