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1.
Food Funct ; 14(15): 7053-7065, 2023 Jul 31.
Article in English | MEDLINE | ID: mdl-37449680

ABSTRACT

Vitamin A, iron, and zinc deficiencies are major nutritional inadequacies in sub-Saharan Africa and disproportionately affect women and children. Biotechnology strategies have been tested to individually improve provitamin A carotenoid or mineral content and/or bioaccessibility in staple crops including sorghum (Sorghum bicolor). However, concurrent carotenoid and mineral enhancement has not been thoroughly assessed and antagonism between these chemical classes has been reported. This work evaluated two genetically engineered constructs containing a suite of heterologous genes to increase carotenoid stability and pathway flux, as well as phytase to catabolize phytate and increase mineral bioaccessibility. Model porridges made from transgenic events were evaluated for carotenoid and mineral content as well as bioaccessibility. Transgenic events produced markedly higher amounts of carotenoids (26.4 µg g-1 DW) compared to null segregants (4.2 µg g-1 DW) and wild-type control (Tx430; 3.7 µg g-1 DW). Phytase activation by pre-steeping flour resulted in significant phytate reduction (9.4 to 4.2 mg g-1 DW), altered the profile of inositol phosphate catabolites, and reduced molar ratios of phytate to iron (16.0 to 4.1), and zinc (19.0 to 4.9) in engineered material, suggesting improved mineral bioaccessibility. Improved phytate : mineral ratios did not significantly affect micellarization and bioaccessible provitamin A carotenoids were over 23 times greater in transgenic events compared to corresponding null segregants and wild-type controls. A 200 g serving of porridge made with these transgenic events provide an estimated 53.7% of a 4-8-year-old child's vitamin A estimated average requirement. These data suggest that combinatorial approaches to enhance micronutrient content and bioaccessibility are feasible and warrant further assessment in human studies.


Subject(s)
6-Phytase , Sorghum , Child , Female , Humans , Child, Preschool , Provitamins/metabolism , Sorghum/chemistry , Vitamin A/metabolism , Phytic Acid/metabolism , 6-Phytase/genetics , 6-Phytase/metabolism , Carotenoids/metabolism , Minerals/metabolism , Iron/metabolism , Zinc/metabolism
2.
Commun Biol ; 5(1): 344, 2022 04 11.
Article in English | MEDLINE | ID: mdl-35410430

ABSTRACT

For many important crops including sorghum, use of CRISPR/Cas technology is limited not only by the delivery of the gene-modification components into a plant cell, but also by the ability to regenerate a fertile plant from the engineered cell through tissue culture. Here, we report that Wuschel2 (Wus2)-enabled transformation increases not only the transformation efficiency, but also the CRISPR/Cas-targeted genome editing frequency in sorghum (Sorghum bicolor L.). Using Agrobacterium-mediated transformation, we have demonstrated Wus2-induced direct somatic embryo formation and regeneration, bypassing genotype-dependent callus formation and significantly shortening the tissue culture cycle time. This method also increased the regeneration capacity that resulted in higher transformation efficiency across different sorghum varieties. Subsequently, advanced excision systems and "altruistic" transformation technology have been developed to generate high-quality morphogenic gene-free and/or selectable marker-free sorghum events. Finally, we demonstrate up to 6.8-fold increase in CRISPR/Cas9-mediated gene dropout frequency using Wus2-enabled transformation, compared to without Wus2, across various targeted loci in different sorghum genotypes.


Subject(s)
Gene Editing , Sorghum , CRISPR-Cas Systems , Edible Grain/genetics , Gene Editing/methods , Plants, Genetically Modified/genetics , Regeneration/genetics , Sorghum/genetics
3.
Int J Mol Sci ; 22(15)2021 Jul 29.
Article in English | MEDLINE | ID: mdl-34360921

ABSTRACT

Hybrid varieties can provide the boost needed to increase stagnant wheat yields through heterosis. The lack of an efficient hybridization system, which can lower the cost of goods of hybrid seed production, has been a major impediment to commercialization of hybrid wheat varieties. In this review, we discuss the progress made in characterization of nuclear genetic male sterility (NGMS) in wheat and its advantages over two widely referenced hybridization systems, i.e., chemical hybridizing agents (CHAs) and cytoplasmic male sterility (CMS). We have characterized four wheat genes, i.e., Ms1, Ms5, TaMs26 and TaMs45, that sporophytically contribute to male fertility and yield recessive male sterility when mutated. While Ms1 and Ms5 are Triticeae specific genes, analysis of TaMs26 and TaMs45 demonstrated conservation of function across plant species. The main features of each of these genes is discussed with respect to the functional contribution of three sub-genomes and requirements for complementation of their respective mutants. Three seed production systems based on three genes, MS1, TaMS26 and TaMS45, were developed and a proof of concept was demonstrated for each system. The Tams26 and ms1 mutants were maintained through a TDNA cassette in a Seed Production Technology-like system, whereas Tams45 male sterility was maintained through creation of a telosome addition line. These genes represent different options for hybridization systems utilizing NGMS in wheat, which can potentially be utilized for commercial-scale hybrid seed production.


Subject(s)
Hybridization, Genetic , Plant Breeding , Plant Infertility/genetics , Plant Proteins/genetics , Pollen/genetics , Triticum , Triticum/genetics , Triticum/growth & development
4.
Plant Sci ; 307: 110899, 2021 Jun.
Article in English | MEDLINE | ID: mdl-33902858

ABSTRACT

Corteva Agriscience™ ran a discovery research program to identify biotech leads for improving maize Agronomic Traits such as yield, drought tolerance, and nitrogen use efficiency. Arising from many discovery sources involving thousands of genes, this program generated over 3331 DNA cassette constructs involving a diverse set of circa 1671 genes, whose transformed maize events were field tested from 2000 to 2018 under managed environments designed to evaluate their potential for commercialization. We demonstrate that a subgroup of these transgenic events improved yield in field-grown elite maize breeding germplasm. A set of at least 22 validated gene leads are identified and described which represent diverse molecular and physiological functions. These leads illuminate sectors of biology that could guide crop improvement in maize and perhaps other crops. In this review and interpretation, we share some of our approaches and results, and key lessons learned in discovering and developing these maize Agronomic Traits leads.


Subject(s)
Biotechnology/methods , Crops, Agricultural/genetics , Gene Expression Regulation, Plant , Genes, Plant , Plant Breeding/methods , Plants, Genetically Modified , Zea mays/genetics , Phenotype
5.
Plant J ; 106(3): 817-830, 2021 05.
Article in English | MEDLINE | ID: mdl-33595147

ABSTRACT

Cowpea (Vigna unguiculata (L.) Walp.) is one of the most important legume crops planted worldwide, but despite decades of effort, cowpea transformation is still challenging due to inefficient Agrobacterium-mediated transfer DNA delivery, transgenic selection and in vitro shoot regeneration. Here, we report a highly efficient transformation system using embryonic axis explants isolated from imbibed mature seeds. We found that removal of the shoot apical meristem from the explants stimulated direct multiple shoot organogenesis from the cotyledonary node tissue. The application of a previously reported ternary transformation vector system provided efficient Agrobacterium-mediated gene delivery, while the utilization of spcN as selectable marker enabled more robust transgenic selection, plant recovery and transgenic plant generation without escapes and chimera formation. Transgenic cowpea plantlets developed exclusively from the cotyledonary nodes at frequencies of 4% to 37% across a wide range of cowpea genotypes. CRISPR/Cas-mediated gene editing was successfully demonstrated. The transformation principles established here could also be applied to other legumes to increase transformation efficiencies.


Subject(s)
Gene Editing/methods , Seeds/genetics , Vigna/genetics , Agrobacterium/genetics , Cotyledon/genetics , Cotyledon/growth & development , Cotyledon/metabolism , Gene Transfer Techniques , Genome, Plant/genetics , Plant Shoots/growth & development , Plants, Genetically Modified , Seeds/growth & development , Seeds/metabolism , Transformation, Genetic , Vigna/growth & development , Vigna/metabolism
6.
Funct Plant Biol ; 48(4): 434-447, 2021 03.
Article in English | MEDLINE | ID: mdl-33332999

ABSTRACT

Hybrid breeding in wheat has the potential to boost yields. An efficient hybrid seed production system requires elite pollinators; however, such germplasm is limited among modern cultivars. Piko, a winter wheat (Triticum aestivum L.) cultivar, has been identified as a superior pollinator and has been used in Europe. Piko has favourable pollinator traits for anther extrusion, anther length, pollen mass and hybrid seed set. However, the genetic factors responsible for Piko's favourable traits are largely unknown. Here, we report on the genetic analysis of a Piko-derived F2 mapping population. We confirmed that Piko's Rht-D1a allele for tall stature is associated with large anthers and high anther extrusion. However, Rht-D1 was not found to be associated with anther filament length, confirmed by near isogenic lines. Piko's photoperiod sensitive Ppd-B1b allele shows an association with increased spike length, more spikelets and spike architecture traits, while the insensitive Ppd-B1a allele is linked with high anther extrusion and larger anthers. We identified an anther extrusion quantitative trait locus (QTL) on chromosome 6A that showed significantly biased transmission of the favourable Piko allele amongst F2 progenies. The Piko allele is completely absent in the distal 6AS region and the central 6A region revealed a significantly lower ratio (<8%) of F2 with homozygous Piko alleles. Our study provided further evidence for the effects of Rht-D1 and Ppd-B1 loci on multiple pollinator traits and a novel anther extrusion QTL that exhibits segregation distortion.


Subject(s)
Plant Breeding , Triticum , Europe , Phenotype , Quantitative Trait Loci/genetics , Triticum/genetics
7.
Plant J ; 99(4): 673-685, 2019 08.
Article in English | MEDLINE | ID: mdl-31009129

ABSTRACT

Nuclear male-sterile mutants with non-conditional, recessive and strictly monogenic inheritance are useful for both hybrid and conventional breeding systems, and have long been a research focus for many crops. In allohexaploid wheat, however, genic redundancy results in rarity of such mutants, with the ethyl methanesulfonate-induced mutant ms5 among the few reported to date. Here, we identify TaMs5 as a glycosylphosphatidylinositol-anchored lipid transfer protein required for normal pollen exine development, and by transgenic complementation demonstrate that TaMs5-A restores fertility to ms5. We show ms5 locates to a centromere-proximal interval and has a sterility inheritance pattern modulated by TaMs5-D but not TaMs5-B. We describe two allelic forms of TaMs5-D, one of which is non-functional and confers mono-factorial inheritance of sterility. The second form is functional but shows incomplete dominance. Consistent with reduced functionality, transcript abundance in developing anthers was found to be lower for TaMs5-D than TaMs5-A. At the 3B homoeolocus, we found only non-functional alleles among 178 diverse hexaploid and tetraploid wheats that include landraces and Triticum dicoccoides. Apparent ubiquity of non-functional TaMs5-B alleles suggests loss-of-function arose early in wheat evolution and, therefore, at most knockout of two homoeoloci is required for sterility. This work provides genetic information, resources and tools required for successful implementation of ms5 sterility in breeding systems for bread and durum wheats.


Subject(s)
Plant Proteins/metabolism , Triticum/metabolism , Carrier Proteins/genetics , Carrier Proteins/metabolism , Plant Infertility/genetics , Plant Infertility/physiology , Plant Proteins/genetics , Pollen/metabolism , Pollen/physiology , Triticum/genetics , Triticum/physiology
8.
Plant Mol Biol ; 97(4-5): 371-383, 2018 Jul.
Article in English | MEDLINE | ID: mdl-29959585

ABSTRACT

KEY MESSAGE: Hexaploid bread wheat is not readily amenable to traditional mutagenesis approaches. In this study, we show efficient utilization of CRISPR-Cas system and Next Generation Sequencing for mutant analysis in wheat. Identification and manipulation of male fertility genes in hexaploid bread wheat is important for understanding the molecular basis of pollen development and to obtain novel sources of nuclear genetic male sterility (NGMS). The maize Male sterile 45 (Ms45) gene encodes a strictosidine synthase-like enzyme and has been shown to be required for male fertility. To investigate the role of Ms45 gene in wheat, mutations in the A, B and D homeologs were produced using CRISPR-Cas9. A variety of mutations in the three homeologs were recovered, including a plant from two different genotypes each with mutations in all three homeologs. Genetic analysis of the mutations demonstrated that all three wheat Ms45 homeologs contribute to male fertility and that triple homozygous mutants are required to abort pollen development and achieve male sterility. Further, it was demonstrated that a wild-type copy of Ms45 gene from rice was able to restore fertility to these wheat mutant plants. Taken together, these observations provide insights into the conservation of MS45 function in a polyploid species. Ms45 based NGMS can be potentially utilized for a Seed Production Technology (SPT)-like hybrid seed production system in wheat.


Subject(s)
CRISPR-Cas Systems , Plant Infertility/genetics , Plant Proteins/metabolism , Triticum/genetics , Amino Acid Sequence , Flowers/genetics , Flowers/growth & development , Mutation , Plant Proteins/genetics , Pollen/genetics , Pollen/growth & development , Sequence Alignment , Triticum/growth & development
9.
Plant Biotechnol J ; 16(7): 1388-1395, 2018 07.
Article in English | MEDLINE | ID: mdl-29327444

ABSTRACT

Sorghum is the fifth most widely planted cereal crop in the world and is commonly cultivated in arid and semi-arid regions such as Africa. Despite its importance as a food source, sorghum genetic improvement through transgenic approaches has been limited because of an inefficient transformation system. Here, we report a ternary vector (also known as cohabitating vector) system using a recently described pVIR accessory plasmid that facilitates efficient Agrobacterium-mediated transformation of sorghum. We report regeneration frequencies ranging from 6% to 29% in Tx430 using different selectable markers and single copy, backbone free 'quality events' ranging from 45% to 66% of the total events produced. Furthermore, we successfully applied this ternary system to develop transformation protocols for popular but recalcitrant African varieties including Macia, Malisor 84-7 and Tegemeo. In addition, we report the use of this technology to develop the first stable CRISPR/Cas9-mediated gene knockouts in Tx430.


Subject(s)
Agrobacterium/genetics , Genetic Engineering/methods , Sorghum/genetics , CRISPR-Cas Systems , Gene Transfer Techniques , Genetic Markers/genetics , Genetic Vectors/genetics , Plants, Genetically Modified/genetics , Transformation, Genetic/genetics
10.
Nat Commun ; 8(1): 869, 2017 10 11.
Article in English | MEDLINE | ID: mdl-29021581

ABSTRACT

The current rate of yield gain in crops is insufficient to meet the predicted demands. Capturing the yield boost from heterosis is one of the few technologies that offers rapid gain. Hybrids are widely used for cereals, maize and rice, but it has been a challenge to develop a viable hybrid system for bread wheat due to the wheat genome complexity, which is both large and hexaploid. Wheat is our most widely grown crop providing 20% of the calories for humans. Here, we describe the identification of Ms1, a gene proposed for use in large-scale, low-cost production of male-sterile (ms) female lines necessary for hybrid wheat seed production. We show that Ms1 completely restores fertility to ms1d, and encodes a glycosylphosphatidylinositol-anchored lipid transfer protein, necessary for pollen exine development. This represents a key step towards developing a robust hybridization platform in wheat.Heterosis can rapidly boost yield in crop species but development of hybrid-breeding systems for bread wheat remains a challenge. Here, Tucker et al. describe the molecular identification of the wheat Ms1 gene and discuss its potential for large-scale hybrid seed production in wheat.


Subject(s)
Carrier Proteins/genetics , Triticum/genetics , Fertility/genetics , Genes, Plant , Genetic Complementation Test , Hybridization, Genetic , Plant Breeding , Plant Proteins/genetics , Pollen/genetics , Pollen/growth & development
11.
Proc Natl Acad Sci U S A ; 113(39): 11040-5, 2016 09 27.
Article in English | MEDLINE | ID: mdl-27621466

ABSTRACT

Micronutrient deficiencies are common in locales where people must rely upon sorghum as their staple diet. Sorghum grain is seriously deficient in provitamin A (ß-carotene) and in the bioavailability of iron and zinc. Biofortification is a process to improve crops for one or more micronutrient deficiencies. We have developed sorghum with increased ß-carotene accumulation that will alleviate vitamin A deficiency among people who rely on sorghum as their dietary staple. However, subsequent ß-carotene instability during storage negatively affects the full utilization of this essential micronutrient. We determined that oxidation is the main factor causing ß-carotene degradation under ambient conditions. We further demonstrated that coexpression of homogentisate geranylgeranyl transferase (HGGT), stacked with carotenoid biosynthesis genes, can mitigate ß-carotene oxidative degradation, resulting in increased ß-carotene accumulation and stability. A kinetic study of ß-carotene degradation showed that the half-life of ß-carotene is extended from less than 4 wk to 10 wk on average with HGGT coexpression.


Subject(s)
Food, Fortified , Sorghum/metabolism , Vitamin E/metabolism , beta Carotene/metabolism , Chromatography, High Pressure Liquid , DNA, Bacterial/genetics , Endosperm/metabolism , Plant Proteins/metabolism , Plants, Genetically Modified , Seeds/metabolism , Sorghum/enzymology , Sorghum/genetics
12.
Plant Biotechnol J ; 14(3): 1046-54, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26442654

ABSTRACT

We have developed a novel hybridization platform that utilizes nuclear male sterility to produce hybrids in maize and other cross-pollinating crops. A key component of this platform is a process termed Seed Production Technology (SPT). This process incorporates a transgenic SPT maintainer line capable of propagating nontransgenic nuclear male-sterile lines for use as female parents in hybrid production. The maize SPT maintainer line is a homozygous recessive male sterile transformed with a SPT construct containing (i) a complementary wild-type male fertility gene to restore fertility, (ii) an α-amylase gene to disrupt pollination and (iii) a seed colour marker gene. The sporophytic wild-type allele complements the recessive mutation, enabling the development of pollen grains, all of which carry the recessive allele but with only half carrying the SPT transgenes. Pollen grains with the SPT transgenes exhibit starch depletion resulting from expression of α-amylase and are unable to germinate. Pollen grains that do not carry the SPT transgenes are nontransgenic and are able to fertilize homozygous mutant plants, resulting in nontransgenic male-sterile progeny for use as female parents. Because transgenic SPT maintainer seeds express a red fluorescent protein, they can be detected and efficiently separated from seeds that do not contain the SPT transgenes by mechanical colour sorting. The SPT process has the potential to replace current approaches to pollen control in commercial maize hybrid seed production. It also has important applications for other cross-pollinating crops where it can unlock the potential for greater hybrid productivity through expanding the parental germplasm pool.


Subject(s)
Crops, Agricultural/genetics , Genes, Recessive , Hybridization, Genetic , Pollination , Seeds/growth & development , Zea mays/genetics , Zea mays/physiology , Biomarkers/metabolism , Fertility , Genes, Plant , Pigmentation/genetics , Plants, Genetically Modified , Transgenes
13.
Proc Nutr Soc ; 74(4): 441-8, 2015 Nov.
Article in English | MEDLINE | ID: mdl-25851095

ABSTRACT

The focus of the review paper is to discuss how biotechnological innovations are opening new frontiers to mitigate nutrition in key agricultural crops with potential for large-scale health impact to people in Africa. The general objective of the Africa Biofortified Sorghum (ABS) project is to develop and deploy sorghum with enhanced pro-vitamin A to farmers and end-users in Africa to alleviate vitamin A-related micronutrient deficiency diseases. To achieve this objective the project technology development team has developed several promising high pro-vitamin A sorghum events. ABS 203 events are so far the most advanced and well-characterised lead events with about 12 µg ß-carotene/g tissue which would supply about 40-50 % of the daily recommended vitamin A at harvest. Through gene expression optimisation other events with higher amounts of pro-vitamin A, including ABS 214, ABS 235, ABS 239 with 25, 30-40, 40-50 µg ß-carotene/g tissue, respectively, have been developed. ABS 239 would provide twice recommended pro-vitamin A at harvest, 50-90 % after 3 months storage and 13-45 % after 6 months storage for children. Preliminary results of introgression of ABS pro-vitamin A traits into local sorghum varieties in target countries Nigeria and Kenya show stable introgression of ABS vitamin A into local farmer-preferred sorghums varieties. ABS gene Intellectual Property Rights and Freedom to Operate have been donated for use royalty free for Africa. Prior to the focus on the current target countries, the project was implemented by fourteen institutions in Africa and the USA. For the next 5 years, the project will complete ABS product development, complete regulatory science data package and apply for product deregulation in target African countries.


Subject(s)
Agriculture , Diet , Edible Grain/chemistry , Food, Genetically Modified , Sorghum/chemistry , Vitamin A Deficiency/prevention & control , beta Carotene/administration & dosage , Biotechnology , Crops, Agricultural , Humans , Kenya , Nigeria , Nutritive Value , Sorghum/genetics , beta Carotene/genetics
14.
Plant Cell Rep ; 33(4): 617-31, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24682459

ABSTRACT

KEY MESSAGE: A high-quality rice activation tagging population has been developed and screened for drought-tolerant lines using various water stress assays. One drought-tolerant line activated two rice glutamate receptor-like genes. Transgenic overexpression of the rice glutamate receptor-like genes conferred drought tolerance to rice and Arabidopsis. Rice (Oryza sativa) is a multi-billion dollar crop grown in more than one hundred countries, as well as a useful functional genetic tool for trait discovery. We have developed a population of more than 200,000 activation-tagged rice lines for use in forward genetic screens to identify genes that improve drought tolerance and other traits that improve yield and agronomic productivity. The population has an expected coverage of more than 90 % of rice genes. About 80 % of the lines have a single T-DNA insertion locus and this molecular feature simplifies gene identification. One of the lines identified in our screens, AH01486, exhibits improved drought tolerance. The AH01486 T-DNA locus is located in a region with two glutamate receptor-like genes. Constitutive overexpression of either glutamate receptor-like gene significantly enhances the drought tolerance of rice and Arabidopsis, thus revealing a novel function of this important gene family in plant biology.


Subject(s)
Adaptation, Physiological/genetics , DNA, Bacterial/genetics , Droughts , Genes, Plant/genetics , Mutagenesis, Insertional/methods , Oryza/genetics , Receptors, Glutamate/genetics , Arabidopsis/genetics , Arabidopsis/physiology , Crosses, Genetic , Gene Expression Regulation, Plant , Genetic Loci , Genome, Plant/genetics , Mutagenesis, Insertional/genetics , Oryza/physiology , Phenotype , Transgenes/genetics
15.
J Agric Food Chem ; 61(24): 5764-71, 2013 Jun 19.
Article in English | MEDLINE | ID: mdl-23692305

ABSTRACT

Biofortified sorghum (Sorghum bicolor (L.) Moench) lines are being developed to target vitamin A deficiency in Sub-Saharan Africa, but the delivery of provitamin A carotenoids from such diverse germplasms has not been evaluated. The purpose of this study was to screen vectors and independent transgenic events for the bioaccessibility of provitamin A carotenoids using an in vitro digestion model. The germplasm background and transgenic sorghum contained 1.0-1.5 and 3.3-14.0 µg/g ß-carotene equivalents on a dry weight basis (DW), respectively. Test porridges made from milled transgenic sorghum contained up to 250 µg of ß-carotene equivalents per 100 g of porridge on a fresh weight basis (FW). Micellarization efficiency of all-trans-ß-carotene was lower (p < 0.05) from transgenic sorghum (1-5%) than from null/nontransgenic sorghum (6-11%) but not different between vector constructs. Carotenoid bioaccessibility was significantly improved (p < 0.05) by increasing the amount of coformulated lipid in test porridges from 5% w/w to 10% w/w. Transgenic sorghum event Homo188-A contained the greatest bioaccessible ß-carotene content, with a 4-8-fold increase from null/nontransgenic sorghum. While the bioavailability and bioconversion of provitamin A carotenoids from these grains must be confirmed in vivo, these data support the notion that biofortification of sorghum can enhance total and bioaccessible provitamin A carotenoid levels.


Subject(s)
Carotenoids/metabolism , Digestion , Models, Biological , Plants, Genetically Modified/chemistry , Seeds/chemistry , Sorghum/chemistry , Vitamin A/metabolism , Carotenoids/analysis , Cooking , Dietary Fats/metabolism , Fatty Acids, Monounsaturated/metabolism , Food Handling , Humans , Micelles , Nutritive Value , Rapeseed Oil , Seeds/genetics , Seeds/metabolism , Sorghum/genetics , Sorghum/metabolism , Vitamin A/analysis , Vitamin A/biosynthesis
16.
Plant Reprod ; 26(2): 125-37, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23539301

ABSTRACT

Expression datasets relating to the Arabidopsis female gametophyte have enabled the creation of a tool set which allows simultaneous visual tracking of each specific cell type (egg, synergids, central cell, and antipodals). This cell-specific, fluorescent labeling tool-set functions from gametophyte cellularization through fertilization and early embryo development. Using this system, cell fates were tracked within Arabidopsis ovules following molecular manipulations, such as the ablation of the egg and/or synergids. Upon egg cell ablation, it was observed that a synergid can switch its developmental fate to become egg/embryo-like upon loss of the native egg. Also, manipulated was the fate of the somatic ovular cells, which can become egg- and embryo-like, reminiscent of adventitious embryony. These advances represent initial steps toward engineering synthetic apomixis resulting in seed derived wholly from the maternal plant. The end goal of applied apomixis research, fixing important agronomic traits such as hybrid vigor, would be a key benefit to agricultural productivity.


Subject(s)
Apomixis/genetics , Arabidopsis/genetics , Arabidopsis/ultrastructure , Gene Expression Regulation, Developmental , Seeds/genetics , Seeds/ultrastructure , Arabidopsis/metabolism , Arabidopsis Proteins/genetics , Arabidopsis Proteins/metabolism , Fertilization , Fluorescence , Gene Expression Regulation, Plant , Genetic Markers , Mutation , Organ Specificity , Ovule/genetics , Ovule/metabolism , Ovule/ultrastructure , Phenotype , Seeds/metabolism
17.
Planta ; 216(5): 778-88, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12624765

ABSTRACT

In normal anther development in maize (Zea mays L), large hypodermal cells in anther primordia undergo a series of proscribed cell divisions to form an anther containing microsporogenous cells and three distinctive anther wall layers: the tapetum, the middle layer and the endothecium. In homozygous msca1 mutants of maize, stamen primordia are initiated normally and large hypodermal cells can be detected in developing anthers. However, the normal series of cell division and differentiation events does not occur in msca1 mutant plants. Rather, structures containing parenchymal cells and ectopic, nonfunctional vascular strands are formed. The epidermal surfaces of these structures contain stomata, which are normally absent in maize anthers. Thus, all of the cell layers of the "anther" have been transformed in mutant plants. The filaments of the mutant structures are normal, and all other flower parts are normal. The msca1 mutation does not affect female fertility, but transformed "stamen" structures remain associated with mature ovules rather than aborting as in normal ear development. The msca1 mutation is distinctive in that only one part of a single (male) reproductive organ is transformed. The resulting structure has general vegetative features, but cannot be conclusively identified as a particular vegetative organ.


Subject(s)
Flowers/genetics , Zea mays/genetics , Fertility/genetics , Fertility/physiology , Flowers/physiology , Flowers/ultrastructure , Gene Expression Regulation, Plant , Homozygote , Microscopy, Electron, Scanning , Mutation , Phenotype , Plants, Genetically Modified , Zea mays/physiology , Zea mays/ultrastructure
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