The rat a-myosin heavy-chain (a-MHC) gene is regulated by 3,5,3'-triiodo-L-thyronine (T3) in ventricular myocardium and is constitutively expressed in atrial tissue. Less is known about regulation of the human gene, but conservation of sequences in the 5'-flanking region between the rat and human a-MHC genes suggests that the human gene may be regulated similarly. Accordingly, T3-responsiveness and tissue-specific expression of human and rat a-MHC/ chloramphenicol acetyltransferase fusion constructs have been compared in rat fetal heart cells, L6E9 myoblasts and myotubes, 3T3 fibroblasts, and HeLa cells. Transient transfection assays revealed a complex series of cis-regulatory elements in the 5'-flanking sequences in the human genes, including a basal promoter element with canonical TATAA and CAAT sequences, two positive regulatory element(s), and two negative regulatory elements, which markedly diminished both constitutive and T3-inducible activity. Interestingly, the human gene seemed to contain a proximal thyroid-hormone response element(s) not found in the rat gene. In L6E9 myoblasts and myotubes, the human constructs were constitutively expressed but not T3-regulated; none of the constructs were active in 3T3 or HeLa cells. We propose that interactions among the thyroid hormone responsive elements and other cis-acting elements in the human a-MHC 5'-flanking sequences may be sufficient to explain the characteristic features of expression of this gene in cardiac tissues.The cardiac myosin heavy chain (MHC) isoforms are the products of two highly homologous genes, a and 1B, which are located in tandem and separated by 4.0 kilobases (kb) of intergenic sequence (1, 2). These genes have distinct patterns of developmental and tissue-specific expression and are subject to modulation by alterations in cardiac workload and hormone status (3-5). Of these multiple regulatory influences, the effects of thyroid hormone are the strongest and best studied (6, 7). In the ventricular myocardium of rats and rabbits, thyroid hormone causes accumulation of a-MHC mRNA and inhibits expression of,-MHC mRNA. It has been proposed that these variations in cardiac myosin isoenzyme may be physiologically important because of a direct relationship between isoform type and the intrinsic speed of muscle contraction-higher speeds of contraction being associated with a predominance of the V1 form (4).Recently, human a-and B-MHC mRNA sequences and their corresponding genes have been isolated and partially characterized (1, 8, 9). The 5'-flanking regions of the rat and human cardiac a-MHC genes show remarkable homology for -600 nucleotides upstream of the putative transcription initiation site, whereas there is little or no homology for the 1000 nucleotides in the 3' direction of the first intron (8). There is, however, very little information available yet about regulation of the human gene. Evidence to date suggests that, like the rat and rabbit genes, the human a-MHC gene is constitutively expressed in atrium (10). Some ventricular...