TY - JOUR
T1 - A mitochondrial-focused genetic interaction map reveals a scaffold-like complex required for inner membrane organization in mitochondria
AU - Hoppins, Suzanne
AU - Collins, Sean R.
AU - Cassidy-Stone, Ann
AU - Hummel, Eric
AU - DeVay, Rachel M.
AU - Lackner, Laura L.
AU - Westermann, Benedikt
AU - Schuldiner, Maya
AU - Weissman, Jonathan S.
AU - Nunnari, Jodi
N1 - National Institutes of Health [R01GM062942, R01GM097432, 1K99HL103722]; Howard Hughes Medical Institute (HHMI); Sandler Asthma Basic Research Center; Helen Hay Whitney FoundationThis work was supported by an National Institutes of Health grants (R01GM062942 and R01GM097432) to J. Nunnari and by support from Howard Hughes Medical Institute (HHMI) and the Sandler Asthma Basic Research Center to J. S. Weissman. S. Hoppins is supported by an National Institutes of Health K99 award (1K99HL103722). S. R. Collins was supported by HHMI and currently holds a Helen Hay Whitney Foundation Fellowship.
PY - 2011/10/17
Y1 - 2011/10/17
N2 - To broadly explore mitochondrial structure and function as well as the communication of mitochondria with other cellular pathways, we constructed a quantitative, high-density genetic interaction map (the MITO-MAP) in Saccharomyces cerevisiae. The MITO-MAP provides a comprehensive view of mitochondrial function including insights into the activity of uncharacterized mitochondrial proteins and the functional connection between mitochondria and the ER. The MITO-MAP also reveals a large inner membrane-associated complex, which we term MitOS for mitochondrial organizing structure, comprised of Fcj1/Mitofilin, a conserved inner membrane protein, and five additional components. MitOS physically and functionally interacts with both outer and inner membrane components and localizes to extended structures that wrap around the inner membrane. We show that MitOS acts in concert with ATP synthase dimers to organize the inner membrane and promote normal mitochondrial morphology. We propose that MitOS acts as a conserved mitochondrial skeletal structure that differentiates regions of the inner membrane to establish the normal internal architecture of mitochondria.
AB - To broadly explore mitochondrial structure and function as well as the communication of mitochondria with other cellular pathways, we constructed a quantitative, high-density genetic interaction map (the MITO-MAP) in Saccharomyces cerevisiae. The MITO-MAP provides a comprehensive view of mitochondrial function including insights into the activity of uncharacterized mitochondrial proteins and the functional connection between mitochondria and the ER. The MITO-MAP also reveals a large inner membrane-associated complex, which we term MitOS for mitochondrial organizing structure, comprised of Fcj1/Mitofilin, a conserved inner membrane protein, and five additional components. MitOS physically and functionally interacts with both outer and inner membrane components and localizes to extended structures that wrap around the inner membrane. We show that MitOS acts in concert with ATP synthase dimers to organize the inner membrane and promote normal mitochondrial morphology. We propose that MitOS acts as a conserved mitochondrial skeletal structure that differentiates regions of the inner membrane to establish the normal internal architecture of mitochondria.
UR - http://www.scopus.com/inward/record.url?scp=80155186698&partnerID=8YFLogxK
U2 - 10.1083/jcb.201107053
DO - 10.1083/jcb.201107053
M3 - مقالة
SN - 0021-9525
VL - 195
SP - 323
EP - 340
JO - Journal of Cell Biology
JF - Journal of Cell Biology
IS - 2
ER -