Original Repository: Stanford University Libraries. Department of Special Collections and University Archives. Paul Berg Papers
Reproduced with permission of Paul Berg.
Medical Subject Headings (MeSH):
Protein Synthesis, Tumor Viruses, and Recombinant DNA, 1959-1975
September 9, 1976
It was a real pleasure to me and talk to you at the Cold Spring Harbor meeting. I see from the program of the Miami Winter
Symposium that we'll have that opportunity again in January.
It seems that both our labs have adopted a similar approach to completing the map of SV40. That's all to the good since
I'm sure that our two sets of findings with the mutants we construct will be sufficient to define the physical limits
and functions of the various genetic elements (structural, regulatory and developmental).
One way to facilitate that would be to keep in touch about what mutants we've obtained and what they do. I know that
you share the view that where practical it would be helpful to exchange mutants between our two labs. In doing so it would
be reasonable to explain the purposes of the exchange so we don't and up trying to do identical experiments and fostering
competition. I'd like to try to develop a more cooperative than competitive arrangement.
If there's any of our deletion mutants you think you could use please feel free to write to me (or call about them. As
I indicated to you when we spoke there are several of the published ones you've made that we'd like to have. Could
we get your early mutants dl 1001, dl 1002 and dl 1009? Luis Villarreal is trying to look at the early SV40 RNA produced
after infection with these mutants and we'd like to include as many mutants with deletions in the early segment as possible.
If you're doing or planning to do the lame experiments perhaps we can work at a way to avoid repetitious efforts.
Another particularly interesting mutant you have reported on is dl 1003 with a deleted - HindII and III fragment F (0.86-.945).
Since Fiers says the VP1 protein has its initiator codon in fragment K it is of interest to know if dl 1003 is B-; we expect
it will be D- and F- but is it B-, and BC-? If it is why? Is there a late RNA made? How big? Is there a 16S RNA made? Is processing
of 19S RNA--16S RNA affected? Perhaps a "16S" RNA is made but can't bind ribosomes to initiate UP1 translation.
Mutant dl 1003 would be useful to sorting out the function of the region just preceding the UP1 structural gene (aside from
the fact that it is probably structural information for UP2 and 3.
I also spoke to you about our efforts to transform cells with DNA and your success was encouraging. Could we get your protocol
and cells (rat and BALB/3T3) to do that? Any advice would be greatly appreciated. Seems many people find DNA mediated transformation
a bit tricky and variable.
I and many of the people at Stanford would love to have you visit. Is there some time prior to January 1, 1977, (I go on sabbatical
just after the first of the year) that you will be out this way or could come to visit and give a seminar? I'd like to
try to find a date for such a visit when I'll be here.