TY - JOUR
T1 - A yeast acetyl coenzyme A carboxylase mutant links very-long-chain fatty acid synthesis to the structure and function of the nuclear membrane-pore complex
AU - Schneiter, Roger
AU - Hitomi, Midori
AU - Ivessa, Andreas S.
AU - Fasch, Evelyn Verena
AU - Kohlwein, Sepp D.
AU - Tartakoff, Alan M.
PY - 1996
Y1 - 1996
N2 - The conditional mRNA transport mutant of Saccharomyces cerevisiae, acc1- 7-1 (mtr7-1), displays a unique alteration of the nuclear envelope. Unlike nucleoporin mutants and other RNA transport mutants, the intermembrane space expands, protuberances extend from the inner membrane into the intermembrane space, and vesicles accumulate in the intermembrane space. MTR7 is the same gene as ACC1, encoding acetyl coenzyme A (CoA) carboxylase (Acc1p), the rate- limiting enzyme of de novo fatty acid synthesis. Genetic and biochemical analyses of fatty acid synthesis mutants and acc1-7-1 indicate that the continued synthesis of malonyl-CoA, the enzymatic product of acetyl-CoA carboxylase, is required for an essential pathway which is independent from de novo synthesis of fatty acids. We provide evidence that synthesis of very- long-chain fatty acids (C26 atoms) is inhibited in acc1-7-1, suggesting that very-long-chain fatty acid synthesis is required to maintain a functional nuclear envelope.
AB - The conditional mRNA transport mutant of Saccharomyces cerevisiae, acc1- 7-1 (mtr7-1), displays a unique alteration of the nuclear envelope. Unlike nucleoporin mutants and other RNA transport mutants, the intermembrane space expands, protuberances extend from the inner membrane into the intermembrane space, and vesicles accumulate in the intermembrane space. MTR7 is the same gene as ACC1, encoding acetyl coenzyme A (CoA) carboxylase (Acc1p), the rate- limiting enzyme of de novo fatty acid synthesis. Genetic and biochemical analyses of fatty acid synthesis mutants and acc1-7-1 indicate that the continued synthesis of malonyl-CoA, the enzymatic product of acetyl-CoA carboxylase, is required for an essential pathway which is independent from de novo synthesis of fatty acids. We provide evidence that synthesis of very- long-chain fatty acids (C26 atoms) is inhibited in acc1-7-1, suggesting that very-long-chain fatty acid synthesis is required to maintain a functional nuclear envelope.
UR - http://www.scopus.com/inward/record.url?scp=0029973561&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0029973561&partnerID=8YFLogxK
U2 - 10.1128/MCB.16.12.7161
DO - 10.1128/MCB.16.12.7161
M3 - Article
C2 - 8943372
AN - SCOPUS:0029973561
SN - 0270-7306
VL - 16
SP - 7161
EP - 7172
JO - Molecular and Cellular Biology
JF - Molecular and Cellular Biology
IS - 12
ER -