The long-term objective of this proposal is to elucidate the biosynthetic and regulatory mechanisms that govern inorganic nitrogen metabolism and signaling. Our previous work has focused on nitrate, which serves as a nutrient and signal for plant growth. This proposal focuses on the synthesis of nitric oxide (NO) and how it serves as a signal in growth and development. NO is an unusual signal in that it is a reactive gas, yet it regulates a large number of cellular and physiological processes including respiration, blood flow and neural development in animals and germination, defence and flowering in plants. In animals NO is made from arginine by nitric oxide synthase (NOS) enzymes. In plants, NO can be made by the reduction of nitrite by the enzyme nitrate reductase. Plants also have an arginine-dependent activity, but no enzyme similar to animal NOS proteins has been identified. We have discovered a gene (AtNOSI) that is needed for arginine- dependent NO synthesis in Arabidopsis. This protein has NOS activity in vitro but is not related to animal NOS in sequence and thus may be a novel NOS. AtNOSI is involved in hormonal signaling, is located in the mitochondria, and is needed for arginine-stimulated NO production by isolated mitochondria. Such synthesis is important as NO regulates mitochondria! functions including respiration, caspase-mediated cell death, and biogenesis, which affects obesity and longevity. There are two sources of mitochondrial NO in animals: eNOS and mtNOS, the identity of the latter being still in question. Because mammalian mitochondria have proteins similar in sequence to AtNOSI, it is possible that AtNOSI-like proteins are or contribute to mtNOS. Our proposal is to investigate the biochemical activity and functions of AtNOSI and its sister genes AtNOS2 and AtNOSS. Specifically, we will determine the biochemical mechanism for NO production by AtNOSI, determine the role of AtNOSI in mitochondrial function, elucidate the role of NO synthesis and AtNOSI function in hormonal signaling, and elucidate the functions and biochemical mechanisms of AtNOS2 and AtNOSS. These studies should shed light on not only the mechanism for NO synthesis used in signaling in plants but also the production of NO in mammalian mitochondria. They also may provide a new mechanism for NO synthesis conserved in plants and animals.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM040672-21
Application #
7742657
Study Section
Cellular Signaling and Dynamics Study Section (CSD)
Program Officer
Maas, Stefan
Project Start
1988-07-01
Project End
2011-11-30
Budget Start
2009-12-01
Budget End
2011-11-30
Support Year
21
Fiscal Year
2010
Total Cost
$330,383
Indirect Cost
Name
University of California San Diego
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
804355790
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Krouk, Gabriel; Ruffel, Sandrine; Gutierrez, Rodrigo A et al. (2011) A framework integrating plant growth with hormones and nutrients. Trends Plant Sci 16:178-82
Wang, Rongchen; Guan, Peizhu; Chen, Mingsheng et al. (2010) Multiple regulatory elements in the Arabidopsis NIA1 promoter act synergistically to form a nitrate enhancer. Plant Physiol 154:423-32
Krouk, Gabriel; Crawford, Nigel M; Coruzzi, Gloria M et al. (2010) Nitrate signaling: adaptation to fluctuating environments. Curr Opin Plant Biol 13:266-73