Bacterial signal peptide recognizes HeLa cell mitochondrial import receptors and functions as a mitochondrial leader sequence

Phage display was used to identify new components of the mammalian mitochondrial receptor complex using Tom20 as a binding partner. Two peptides were identified. One had partial identity (SMLTVMA) with a bacterial signal peptide from Toho-1, a periplasmic protein. The other had partial identity with a mitochondrial inner membrane glutamate carrier. The bacterial signal peptide could carry a protein into mitochondria both in vivo and in vitro. The first six residues of the sequence, SMLTVM, were necessary for import but the two adjacent arginine residues in the 30-amino-acid leader were not critical for import. The signal peptides of Escherichia coli β-lactamase and Bacillsus subtilis lipase could not carry proteins into mitochondria. Presumably, the Toho-1 leader can adopt a structure compatible for recognition by the import apparatus.Received 29 April 2005; received after revision 8 June 2005; accepted 17 June 2005     

Homologies ofNeurospora homothallic species using repeated and nonrepeated DNA sequences

Summary DNA:DNA hybridization studies of the homothallic species ofNeurospora showed that the repeated DNA sequences provided no means of distinction among them. Hybridization with nonrepeated DNA sequences, however, showed that theN. terricola species was quite unlike the others. These studies suggest that heterothallism might have evolved from homothallism inNeurospora.Supported in part by a contract with the US Department of Energy. We are grateful to Dr Lafayette Frederick of this Department for helping us with the cultures ofN. terricola andN. galapagosensis.