Tie-dyed1 regulates carbohydrate accumulation in maize leaves

被引:55
作者
Braun, David M. [1 ]
Ma, Yi
Inada, Noriko
Muszynski, Michael G.
Baker, R. Frank
机构
[1] Penn State Univ, Dept Biol, University Pk, PA 16802 USA
[2] Univ Calif Berkeley, Dept Plant & Microbial Biol, Berkeley, CA 94720 USA
[3] Pioneer HiBred Int Inc, Dept Agron, Johnston, IA 50131 USA
关键词
D O I
10.1104/pp.106.090381
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Acquisition of cell identity requires communication among neighboring cells. To dissect the genetic pathways regulating cell signaling in later leaf development, a screen was performed to identify mutants with chloroplast pigmentation sectors that violate cell lineage boundaries in maize (Zea mays) leaves. We have characterized a recessive mutant, tie-dyed1 (tdy1), which develops stable, nonclonal variegated yellow and green leaf sectors. Sector formation requires high light, occurs during a limited developmental time, and is restricted to leaf blade tissue. Yellow tdy1 sectors accumulate excessive soluble sugars and starch, whereas green sectors appear unaffected. Significantly, starch accumulation precedes chlorosis in cells that will become a yellow sector. Retention of carbohydrates in tdy1 leaves is associated with a delay in reproductive maturity, decreased stature, and reduced yield. To explain the tdy1 sectoring pattern, we propose a threshold model that incorporates the light requirement and the hyperaccumulation of photoassimilates. A possible function consistent with this model is that TDY1 acts as a sugar sensor to regulate an inducible sugar export pathway as leaves develop under high light conditions.
引用
收藏
页码:1511 / 1522
页数:12
相关论文
共 53 条
[42]   METABOLIC REPRESSION OF TRANSCRIPTION IN HIGHER-PLANTS [J].
SHEEN, J .
PLANT CELL, 1990, 2 (10) :1027-1038
[43]   A LOW-VISCOSITY EPOXY RESIN EMBEDDING MEDIUM FOR ELECTRON MICROSCOPY [J].
SPURR, AR .
JOURNAL OF ULTRASTRUCTURE RESEARCH, 1969, 26 (1-2) :31-&
[44]  
SYLVESTER AW, 1990, DEVELOPMENT, V110, P985
[45]   Acquisition of identity in the developing leaf [J].
Sylvester, AW ;
Smith, L ;
Freeling, M .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1996, 12 :257-304
[46]   THE SINK-SOURCE TRANSITION IN LEAVES [J].
TURGEON, R .
ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY, 1989, 40 :119-138
[47]   Deletion of the chloroplast-localized Thylakoid formation1 gene product in Arabidopsis leads to deficient thylakoid formation and variegated leaves [J].
Wang, Q ;
Sullivan, RW ;
Kight, A ;
Henry, RL ;
Huang, JR ;
Jones, AM ;
Korth, KL .
PLANT PHYSIOLOGY, 2004, 136 (03) :3594-3604
[48]   A new subfamily of sucrose transporters, SUT4, with low affinity/high capacity localized in enucleate sieve elements of plants [J].
Weise, A ;
Barker, L ;
Kühn, C ;
Lalonde, S ;
Buschmann, H ;
Frommer, WB ;
Ward, JM .
PLANT CELL, 2000, 12 (08) :1345-1355
[49]   NUCLEAR ORGANELLE INTERACTIONS - THE IMMUTANS VARIEGATION MUTANT OF ARABIDOPSIS IS PLASTID AUTONOMOUS AND IMPAIRED IN CAROTENOID BIOSYNTHESIS [J].
WETZEL, CM ;
JIANG, CZ ;
MEEHAN, LJ ;
VOYTAS, DF ;
RODERMEL, SR .
PLANT JOURNAL, 1994, 6 (02) :161-175
[50]   The immutans variegation locus of Arabidopsis defines a mitochondrial alternative oxidase homolog that functions during early chloroplast biogenesis [J].
Wu, DY ;
Wright, DA ;
Wetzel, C ;
Voytas, DF ;
Rodermel, S .
PLANT CELL, 1999, 11 (01) :43-55