The DNA coding for RNase H from a mutant strain of Escherichia coli (FB2) was cloned into plasmid pBR322. DNA sequence analysis and the exchange of a portion of the mutant and wild-type genes revealed that a single-base alteration (C-->T) in the coding region of the structural gene for RNase H is responsible for the difference in RNase H activity of the wild-type and mutant cells.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC217564PMC
http://dx.doi.org/10.1128/jb.154.2.1021-1026.1983DOI Listing

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