Maize opaque endosperm mutations create extensive changes in patterns of gene expression

被引:143
作者
Hunter, BG
Beatty, MK
Singletary, GW
Hamaker, BR
Dilkes, BP
Larkins, BA
Jung, R [1 ]
机构
[1] Univ Arizona, Dept Plant Sci, Tucson, AZ 85721 USA
[2] Pioneer HiBred Int Inc, Johnston, IA 50131 USA
[3] Purdue Univ, Dept Food Sci, W Lafayette, IN 47907 USA
关键词
D O I
10.1105/tpc.003905
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Maize starchy endosperm mutants have kernel phenotypes that include a brittle texture, susceptibility to insect pests, and inferior functional characteristics of products made from their flour. At least 18 such mutants have been identified, but only in the cases of opaque2 (o2) and floury2 (fl2), which affect different aspects of storage protein synthesis, is the molecular basis of the mutation known. To better understand the relationship between the phenotypes of these mutants and their biochemical bases, we characterized the protein and amino acid composition, as well as the mRNA transcript profiles, of nearly isogenic inbred lines of W64A o1, o2, o5, o9, o11, Mucuronate (Mc), Defective endosperm B30 (DeB30), and fl2. The largest reductions in zein protein synthesis occur in the W64A o2, DeB30, and fl2 mutants, which have similar to35 to 55% of the wild-type level of storage proteins. Zeins in W64A o5, o9, o11, and Mc are within 80 to 90% of the amount found in the wild type. Only in the cases of o5 and Mc were significant qualitative changes in zein synthesis observed. The pattern of gene expression in normal and mutant genotypes was assayed by profiling endosperm mRNA transcripts at 18 days after pollination with an Affymetrix GeneChip containing >1400 selected maize gene sequences. Compared with W64A sugary1, a mutant defective in starch synthesis, alterations in the gene expression patterns of the opaque mutants are very pleiotropic. Increased expression of genes associated with physiological stress, and the unfolded protein response, are common features of the opaque mutants. Based on global patterns of gene expression, these mutants were categorized in four phenotypic groups as follows: W64A+ and o1; o2; o5/o9/o11; and Mc and fl2.
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收藏
页码:2591 / 2612
页数:22
相关论文
共 53 条
[11]  
DOEHLERT DC, 1994, PLANT CELL PHYSIOL, V35, P411
[12]   Cluster analysis and display of genome-wide expression patterns [J].
Eisen, MB ;
Spellman, PT ;
Brown, PO ;
Botstein, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14863-14868
[13]   CHARACTERIZATION OF AN IMMUNOGLOBULIN BINDING-PROTEIN HOMOLOG IN THE MAIZE FLOURY-2 ENDOSPERM MUTANT [J].
FONTES, EBP ;
SHANK, BB ;
WROBEL, RL ;
MOOSE, SP ;
OBRIAN, GR ;
WURTZEL, ET ;
BOSTON, RS .
PLANT CELL, 1991, 3 (05) :483-496
[14]   OPAQUE-2 MODIFIERS INCREASE GAMMA-ZEIN SYNTHESIS AND ALTER ITS SPATIAL-DISTRIBUTION IN MAIZE ENDOSPERM [J].
GEETHA, KB ;
LENDING, CR ;
LOPES, MA ;
WALLACE, JC ;
LARKINS, BA .
PLANT CELL, 1991, 3 (11) :1207-1219
[15]   A defective signal peptide tethers the floury-2 zein to the endoplasmic reticulum membrane [J].
Gillikin, JW ;
Zhang, F ;
Coleman, CE ;
Bass, HW ;
Larkins, BA ;
Boston, RS .
PLANT PHYSIOLOGY, 1997, 114 (01) :345-352
[16]   COORDINATED TRANSCRIPTIONAL REGULATION OF STORAGE PRODUCT GENES IN THE MAIZE ENDOSPERM [J].
GIROUX, MJ ;
BOYER, C ;
FEIX, G ;
HANNAH, LC .
PLANT PHYSIOLOGY, 1994, 106 (02) :713-722
[17]   THE ORIGIN OF LYSINE-CONTAINING PROTEINS IN OPAQUE-2 MAIZE ENDOSPERM [J].
HABBEN, JE ;
KIRLEIS, AW ;
LARKINS, BA .
PLANT MOLECULAR BIOLOGY, 1993, 23 (04) :825-838
[18]   ELONGATION-FACTOR 1-ALPHA CONCENTRATION IS HIGHLY CORRELATED WITH THE LYSINE CONTENT OF MAIZE ENDOSPERM [J].
HABBEN, JE ;
MORO, GL ;
HUNTER, BG ;
HAMAKER, BR ;
LARKINS, BA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (19) :8640-8644
[19]   Resistance gene-dependent plant defense responses [J].
HammondKosack, KE ;
Jones, JDG .
PLANT CELL, 1996, 8 (10) :1773-1791
[20]   CHARACTERIZATION OF THE MAIZE GENE SUGARY1, A DETERMINANT OF STARCH COMPOSITION IN KERNELS [J].
JAMES, MG ;
ROBERTSON, DS ;
MYERS, AM .
PLANT CELL, 1995, 7 (04) :417-429