The genes that code for two allotypic forms ofthe rat Kc light chain constant region (CM) have been cloned and the nucleotide sequence of 1172 base pairs of coding and flanking sequence has been determined for both alleles. These sequences have been compared to each other and to the corresponding sequences found in the mouse and human. Comparison of the LEW allele with mouse CK reveals two surprising features: (i) There is an unusually large number ofamino acid substitutions (21) relative to the total number ofnucleotide changes (37) in the coding region. Comparison among several other mammalian genes reveals a larger proportion of"silent" changes. (ii) The rate ofaccumulation of base substitutions is the same within the coding region as it is in some 870 base pairs of noncoding sequence (including 3' untranslated, 3' flanking, and 5' intervening sequences). Comparison of the two allelic forms of rat CK shows the same unusual features in more extreme form. (i) Twelve base substitutions in the coding region determine 11 amino acid differences-only one "silent" change exists. (ii) There are 12 base substitutions in the 318 base pairs of coding sequence (3.7% difference) and only 9 in the remaining 854 base pairs of noncoding DNA (1.1%), a highly significant difference. This degree of conservation of noncoding sequences and of "silent" sites within the coding region is unique among the mammalian genes studied thus far. These patterns suggest that there has been strong selection for conservation of nucleotide sequences, both inside and outside the coding region, independent of the selection required to maintain the function and characteristic structure of the immunoglobulin domain itself. The functions ofthe nucleotide sequences that account for this selective pressure are unclear at the present time.There are now a number of mammalian genes for which nucleotide sequences have been determined, including insulin (1), growth hormone (2), various globin genes (3), dihydrofolate reductase (4), and immunoglobulin heavy and light chains (5). For some of these genes the sequence has been determined in several species, allowing interspecific comparisons (3,(6)(7)(8) MATERIALS AND METHODS Mouse Probe. The probe used for the isolation of the rat C, genes was obtained from Jonathan Seidman (Philip Leder's laboratory, National Institutes of Health) and is designated K41-C (11). This probe consists of the plasmid pBR322 with inserted mouse cDNA corresponding to the constant region ofthe K type immunoglobulin light chain from the MOPC-41 plasmacytoma. The DNA, inserted at the BamHI restriction endonuclease site of pBR322, consists of the coding region starting at amino acid 125, through the 3' end of the mRNA [including the untranslated region and poly(A)] with BamHI synthetic linkers at each end. For these studies, the BamHI insert was purified and labeled by nick translation to a specific activity ofgreater than 108 cpm/lg. Genomic Blot. High molecular weight DNA was prepared from adult rat liver according to Blin and...