TY - JOUR
T1 - Tim18p is a new component of the Tim54p-Tim22p translocon in the mitochondrial inner membrane
AU - Kerscher, Oliver
AU - Sepuri, Naresh B.
AU - Jensen, Robert E.
PY - 2000/1
Y1 - 2000/1
N2 - The mitochondrial inner membrane contains two separate translocons: one required for the translocation of matrix-targeted proteins (the Tim23p-Tim17p complex) and one for the insertion of polytopic proteins into the mitochondrial inner membrane (the Tim54p-Tim22p complex). To identify new members of the Tim54p-Tim22p complex, we screened for high-copy suppressors of the temperature-sensitive tim54-1 mutant. We identified a new gene, TIM18, that encodes an integral protein of the inner membrane. The following genetic and biochemical observations suggest that the Tim18 protein is part of the Tim54p-Tim22p complex in the inner membrane: multiple copies of TIM18 suppress the tim54-1 growth defect; the tim18::HIS3 disruption is synthetically lethal with tim54-1; Tim54p and Tim22p can be coimmune precipitated with the Tim18 protein; and Tim18p, along with Tim54p and Tim22p, is detected in an ~300-kDa complex after blue native electrophoresis. We propose that Tim18p is a new component of the Tim54pTim22p machinery that facilitates insertion of polytopic proteins into the mitochondrial inner membrane.
AB - The mitochondrial inner membrane contains two separate translocons: one required for the translocation of matrix-targeted proteins (the Tim23p-Tim17p complex) and one for the insertion of polytopic proteins into the mitochondrial inner membrane (the Tim54p-Tim22p complex). To identify new members of the Tim54p-Tim22p complex, we screened for high-copy suppressors of the temperature-sensitive tim54-1 mutant. We identified a new gene, TIM18, that encodes an integral protein of the inner membrane. The following genetic and biochemical observations suggest that the Tim18 protein is part of the Tim54p-Tim22p complex in the inner membrane: multiple copies of TIM18 suppress the tim54-1 growth defect; the tim18::HIS3 disruption is synthetically lethal with tim54-1; Tim54p and Tim22p can be coimmune precipitated with the Tim18 protein; and Tim18p, along with Tim54p and Tim22p, is detected in an ~300-kDa complex after blue native electrophoresis. We propose that Tim18p is a new component of the Tim54pTim22p machinery that facilitates insertion of polytopic proteins into the mitochondrial inner membrane.
UR - http://www.scopus.com/inward/record.url?scp=0033963688&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0033963688&partnerID=8YFLogxK
U2 - 10.1091/mbc.11.1.103
DO - 10.1091/mbc.11.1.103
M3 - Article
C2 - 10637294
AN - SCOPUS:0033963688
SN - 1059-1524
VL - 11
SP - 103
EP - 116
JO - Molecular biology of the cell
JF - Molecular biology of the cell
IS - 1
ER -