The mitochondrial NAD+ transporter (NDT1) plays important roles in cellular NAD+ homeostasis in Arabidopsis thaliana

被引:34
作者
Chaves, Izabel de Souza [1 ]
Feitosa-Araujo, Elias [1 ]
Florian, Alexandra [2 ]
Medeiros, David B. [1 ]
da Fonseca-Pereira, Paula [1 ]
Charton, Lennart [3 ]
Heyneke, Elmien [2 ]
Apfata, Jorge A. C. [1 ]
Pires, Marcel, V [1 ]
Mettler-Altmann, Tabea [3 ]
Araujo, Wagner L. [1 ]
Neuhaus, H. Ekkehard [4 ]
Palmieri, Ferdinando [5 ]
Obata, Toshihiro [2 ]
Weber, Andreas P. M. [3 ]
Linka, Nicole [3 ]
Fernie, Alisdair R. [2 ]
Nunes-Nesi, Adriano [1 ,2 ]
机构
[1] Univ Fed Vicosa, Dept Biol Vegetal, Max Planck Partner Grp, BR-36570900 Vicosa, MG, Brazil
[2] Max Planck Inst Mol Plant Physiol, Muhlenberg 1, D-14476 Potsdam, Germany
[3] Heinrich Heine Univ Dusseldorf, Dept Plant Biochem, D-40225 Dusseldorf, Germany
[4] Univ Kaiserslautern, Dept Plant Physiol, D-67663 Kaiserslautern, Germany
[5] Univ Bari, Dept Biosci Biotechnol & Biopharmaceut, I-70125 Bari, Italy
关键词
Arabidopsis thaliana; nicotinamide adenine dinucleotide; transporter; pollen viability; starch metabolism; ENERGY HOMEOSTASIS; ENZYME-ACTIVITIES; COFFEA-CANEPHORA; OXIDATIVE STRESS; DIURNAL CYCLES; PLANTS; POLLEN; METABOLISM; KINASE; DEHYDROGENASE;
D O I
10.1111/tpj.14452
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Nicotinamide adenine dinucleotide (NAD(+)) is an essential coenzyme required for all living organisms. In eukaryotic cells, the final step of NAD(+) biosynthesis is exclusively cytosolic. Hence, NAD(+) must be imported into organelles to support their metabolic functions. Three NAD(+) transporters belonging to the mitochondrial carrier family (MCF) have been biochemically characterized in plants. AtNDT1 (At2g47490), focus of the current study, AtNDT2 (At1g25380), targeted to the inner mitochondrial membrane, and AtPXN (At2g39970), located in the peroxisomal membrane. Although AtNDT1 was presumed to reside in the chloroplast membrane, subcellular localization experiments with green fluorescent protein (GFP) fusions revealed that AtNDT1 locates exclusively in the mitochondrial membrane in stably transformed Arabidopsis plants. To understand the biological function of AtNDT1 in Arabidopsis, three transgenic lines containing an antisense construct of AtNDT1 under the control of the 35S promoter alongside a T-DNA insertional line were evaluated. Plants with reduced AtNDT1 expression displayed lower pollen viability, silique length, and higher rate of seed abortion. Furthermore, these plants also exhibited an increased leaf number and leaf area concomitant with higher photosynthetic rates and higher levels of sucrose and starch. Therefore, lower expression of AtNDT1 was associated with enhanced vegetative growth but severe impairment of the reproductive stage. These results are discussed in the context of the mitochondrial localization of AtNDT1 and its important role in the cellular NAD(+) homeostasis for both metabolic and developmental processes in plants.
引用
收藏
页码:487 / 504
页数:18
相关论文
共 69 条
[1]   The phosphate makes a difference: cellular functions of NADP [J].
Agledal, Line ;
Niere, Marc ;
Ziegler, Mathias .
REDOX REPORT, 2010, 15 (01) :2-10
[2]   The peroxisomal NAD+ carrier of Arabidopsis thaliana transports coenzyme A and its derivatives [J].
Agrimi, Gennaro ;
Russo, Annamaria ;
Pierri, Ciro Leonardo ;
Palmieri, Ferdinando .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 2012, 44 (03) :333-340
[3]   Development of a database of gas chromatographic retention properties of organic compounds [J].
Babushok, V. I. ;
Linstrom, P. J. ;
Reed, J. J. ;
Zenkevich, I. G. ;
Brown, R. L. ;
Mallard, W. G. ;
Stein, S. E. .
JOURNAL OF CHROMATOGRAPHY A, 2007, 1157 (1-2) :414-421
[4]   An integrated overview of seed development in Arabidopsis thaliana ecotype WS [J].
Baud, S ;
Boutin, JP ;
Miquel, M ;
Lepiniec, L ;
Rochat, C .
PLANT PHYSIOLOGY AND BIOCHEMISTRY, 2002, 40 (02) :151-160
[5]  
BECHTOLD N, 1993, CR ACAD SCI III-VIE, V316, P1194
[6]   Folate metabolism in plants -: An Arabidopsis homolog of the mammalian mitochondrial folate transporter mediates folate import into chloroplasts [J].
Bedhomme, M ;
Hoffmann, M ;
McCarthy, EA ;
Gambonnet, B ;
Moran, RG ;
Rébeillé, F ;
Ravanel, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (41) :34823-34831
[7]   A peroxisomal carrier delivers NAD plus and contributes to optimal fatty acid degradation during storage oil mobilization [J].
Bernhardt, Kristin ;
Wilkinson, Sabrina ;
Weber, Andreas P. M. ;
Linka, Nicole .
PLANT JOURNAL, 2012, 69 (01) :1-13
[8]   Stress induces the expression of AtNADK-1, a gene encoding a NAD(H) kinase in Arabidopsis thaliana [J].
Berrin, JG ;
Pierrugues, O ;
Brutesco, C ;
Alonso, B ;
Montillet, JL ;
Roby, D ;
Kazmaier, M .
MOLECULAR GENETICS AND GENOMICS, 2005, 273 (01) :10-19
[9]   The effect of G1c6P uptake and its subsequent oxidation within pea root plastids on nitrite reduction and glutamate synthesis [J].
Bowsher, Caroline G. ;
Lacey, Anne E. ;
Hanke, Guy T. ;
Clarkson, David T. ;
Saker, Les R. ;
Stulen, Ineke ;
Emes, Michael J. .
JOURNAL OF EXPERIMENTAL BOTANY, 2007, 58 (05) :1109-1118
[10]   FATTY-ACID COMPOSITION OF LEAF LIPIDS DETERMINED AFTER COMBINED DIGESTION AND FATTY-ACID METHYL-ESTER FORMATION FROM FRESH TISSUE [J].
BROWSE, J ;
MCCOURT, PJ ;
SOMERVILLE, CR .
ANALYTICAL BIOCHEMISTRY, 1986, 152 (01) :141-145