TY - JOUR
T1 - Characterization of Arabidopsis NEET reveals an ancient role for NEET proteins in iron metabolism
AU - Nechushtai, Rachel
AU - Conlan, Andrea R.
AU - Harir, Yael
AU - song, Luhua
AU - yogev, ohad
AU - Eisenberg-Domovich, Yael
AU - Livnah, Oded
AU - Michaeli, Dorit
AU - Rosen, Rachel
AU - Ma, Vincent
AU - Luo, Yuting
AU - Zuris, John A.
AU - Paddock, Mark L.
AU - Cabantchik, Zvi Ioav
AU - Jennings, Patricia A.
AU - Mittler, Ron
PY - 2012/5
Y1 - 2012/5
N2 - The NEET family is a newly discovered group of proteins involved in a diverse array of biological processes, including autophagy, apoptosis, aging, diabetes, and reactive oxygen homeostasis. They form a novel structure, the NEET fold, in which two protomers intertwine to form a two-domain motif, a cap, and a unique redox-active labile 2Fe-2S cluster binding domain. To accelerate the functional study of NEET proteins, as well as to examine whether they have an evolutionarily conserved role, we identified and characterized a plant NEET protein. Here, we show that the Arabidopsis thaliana At5g51720 protein (At-NEET) displays biochemical, structural, and biophysical characteristics of a NEET protein. Phenotypic characterization of At-NEET revealed a key role for this protein in plant development, senescence, reactive oxygen homeostasis, and Fe metabolism. A role in Fe metabolism was further supported by biochemical and cell biology studies of At-NEET in plant and mammalian cells, as well as mutational analysis of its cluster binding domain. Our findings support the hypothesis that NEET proteins have an ancient role in cells associated with Fe metabolism.
AB - The NEET family is a newly discovered group of proteins involved in a diverse array of biological processes, including autophagy, apoptosis, aging, diabetes, and reactive oxygen homeostasis. They form a novel structure, the NEET fold, in which two protomers intertwine to form a two-domain motif, a cap, and a unique redox-active labile 2Fe-2S cluster binding domain. To accelerate the functional study of NEET proteins, as well as to examine whether they have an evolutionarily conserved role, we identified and characterized a plant NEET protein. Here, we show that the Arabidopsis thaliana At5g51720 protein (At-NEET) displays biochemical, structural, and biophysical characteristics of a NEET protein. Phenotypic characterization of At-NEET revealed a key role for this protein in plant development, senescence, reactive oxygen homeostasis, and Fe metabolism. A role in Fe metabolism was further supported by biochemical and cell biology studies of At-NEET in plant and mammalian cells, as well as mutational analysis of its cluster binding domain. Our findings support the hypothesis that NEET proteins have an ancient role in cells associated with Fe metabolism.
UR - http://www.scopus.com/inward/record.url?scp=84863325942&partnerID=8YFLogxK
U2 - 10.1105/tpc.112.097634
DO - 10.1105/tpc.112.097634
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AN - SCOPUS:84863325942
SN - 1040-4651
VL - 24
SP - 2139
EP - 2154
JO - Plant Cell
JF - Plant Cell
IS - 5
ER -