Fertility alteration in the photo-thermo-sensitive male sterile line BS20 of wheat (Triticum aestivum L.)

Male sterility is a valuable trait for genetic research and production application of wheat (Triticum aestivum L.). NWMS1, a novel typical genic male sterility mutant, was obtained from Shengnong 1, mutagenized with ethyl methane sulfonate (EMS). Microstructure and ultrastructure observations of the anthers and microspores indicated that the pollen abortion of NWMS1 started at the early uninucleate microspore stage. Pollen grain collapse, plasmolysis, and absent starch grains were the three typical characteristics of the abnormal microspores. The anther transcriptomes of NWMS1 and its wild type Shengnong 1 were compared at the early anther development stage, pollen mother cell meiotic stage, and binucleate microspore stage. Several biological pathways clearly involved in abnormal anther development were identified, including protein processing in endoplasmic reticulum, starch and sucrose metabolism, lipid metabolism, and plant hormone signal transduction. There were 20 key genes involved in the abnormal anther development, screened out by weighted gene co-expression network analysis (WGCNA), including SKP1B, BIP5, KCS11, ADH3, BGLU6, and TIFY10B. The results indicated that the defect in starch and sucrose metabolism was the most important factor causing male sterility in NWMS1. Based on the experimental data, a primary molecular regulation model of abnormal anther and pollen developments in mutant NWMS1 was established. These results laid a solid foundation for further research on the molecular mechanism of wheat male sterility.

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Inheritance of the blue aleurone trait in diverse wheat crosses

Genome ◽

10.1139/g90-078 ◽

1990 ◽

Vol 33 (4) ◽

pp. 525-529 ◽

Cited By ~ 22

Author(s):

V. D. Keppenne ◽

P. S. Baenziger

Keyword(s):

Triticum Aestivum ◽

Genetic Marker ◽

Dominant Gene ◽

Triticum Aestivum L ◽

Progeny Testing ◽

Seed Color ◽

Male Sterile ◽

Agropyron Elongatum ◽

Doubled Haploidy ◽

Wheat Lines

The blue aleurone trait has been suggested as a useful genetic marker in wheat (Triticum aestivum L.). However, little information is available on its transmission in diverse backgrounds and on its use to identify hybrid seed. UC66049, a hexaploid spring wheat with a spontaneous translocation that included the gene for the blue aleurone trait (Ba) from Agropyron elongatum (Host) P.B. (synonymous with Elytrigia pontica (Podp.) Holub), was crossed to seven wheat cultivars to test the transmission of the trait. UC66049 was crossed to male-sterile red wheat lines to evaluate the blue aleurone trait as a marker for confirming hybridity. Ba segregated as a dominant gene that was transmitted normally through the male and female gametes. For 6 of 7 crosses with diverse pedigrees, we experienced problems with misclassification of the aleurone color in the F2 seed generation, determined by the F3 seed family data. The blue aleurone trait is a good genetic marker; however, progeny testing may be needed to confirm the F2 genotypes in some environments or genetic backgrounds. Moreover, Ba is useful in determining the amount of controlled hybridity as opposed to self-fertility and (or) outcrossing in genetic male-sterile wheat lines. The use of Ba to confirm doubled haploidy was proposed.Key words: Agropyron elongatum, seed color, genetics, Triticum aestivum, Elytrigia pontica.

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Comprehensive analysis of polygalacturonase family highlights candidate genes related to pollen development and male fertility in wheat (Triticum aestivum L.)

10.21203/rs.2.18306/v1 ◽

2019 ◽

Author(s):

Jiali Ye ◽

Xuetong Yang ◽

Zhiquan Yang ◽

Wei Li ◽

Qi Liu ◽

...

Keyword(s):

Triticum Aestivum ◽

Gene Family ◽

Candidate Genes ◽

Pollen Development ◽

Male Fertility ◽

Triticum Aestivum L ◽

Segmental Duplications ◽

Rna Seq ◽

Male Sterile ◽

Wide Range

Abstract Background: Polygalacturonase (PG) belongs to a large family of hydrolases with important functions in cell separation during plant growth and development via the degradation of pectin. The specific expression of PG genes in anthers may be significant for male sterility research and hybrid wheat breeding, but it has not been characterized in wheat (Triticum aestivum L.). Results: We systematically studied the PG gene family using the latest published wheat reference genomic information. In total, 113 wheat PG genes were identified and renamed as TaPG01–113 based on their chromosomal positions. The PG genes are unequally distributed on 21 chromosomes and classified according to six categories from A–F. Analysis of the gene structures and conserved motifs demonstrated that the Class C and D TaPGs have relatively short gene sequences and a small number of introns. Class E TaPGs are the least conserved and lack conserved domain III. Polyploidy and segmental duplications in wheat were mainly responsible for the expansion of the wheat PG gene family. Predictions of cis-elements indicate that TaPGs have a wide range of functions, including the responses to light, hypothermia, anaerobic conditions, and hormonal stimulation, as well as being involved in meristematic tissue expression. RNA-seq showed that TaPGs have specific temporal and spatial expression characteristics. Twelve spike-specific TaPGs were screened using RNA-seq data and verified by qRT-PCR in the sterile and fertile anthers of thermo-sensitive male-sterile wheat. Four important candidate genes were identified as involved in the male fertility determination process. In fertile anthers, TaPG09 may be involved in the separation of pollen. TaPG87 and TaPG95 could play important roles in anther dehiscence. TaPG93 may be related to pollen development and pollen tube elongation. Conclusions: We analyzed the wheat PG gene family and identified four important TaPGs with differential expression levels in the wheat fertility conversion process. Our findings may facilitate functional investigations of the wheat PG gene family and provide new insights into the fertility conversion mechanism in male-sterile wheat.

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Phenotype characterisation and analysis of expression patterns of genes related mainly to carbohydrate metabolism and sporopollenin in male-sterile anthers induced by high temperature in wheat (Triticum aestivum)

Crop and Pasture Science ◽

10.1071/cp18034 ◽

2018 ◽

Vol 69 (5) ◽

pp. 469 ◽

Cited By ~ 4

Author(s):

Hongzhan Liu ◽

Junsheng Wang ◽

Chaoqiong Li ◽

Lin Qiao ◽

Xueqin Wang ◽

...

Keyword(s):

Triticum Aestivum ◽

High Temperature ◽

Male Sterility ◽

Carbohydrate Metabolism ◽

Higher Plants ◽

Expression Patterns ◽

Triticum Aestivum L ◽

Male Sterile ◽

Tetrad Stage ◽

Expression Levels

Male reproductive development in higher plants is highly sensitive to various stressors, including high temperature (HT). In this study, physiological male-sterile plants of wheat (Triticum aestivum L.) were established using HT induction. The physiological changes and expression levels of genes mainly related to carbohydrate metabolism and sporopollenin in male-sterile processes were studied by using biological techniques, including iodine–potassium iodide staining, paraffin sectioning, scanning electron microscopy (SEM) and fluorescent quantitative analysis. Results of paraffin sectioning and SEM revealed that parts of HT male-sterile anthers, including the epidermis and tapetum, were remarkably different from those of normal anthers. The expression levels of TaSUT1, TaSUT2, IVR1 and IVR5 were significantly lower than of normal anthers at the early microspore and trinucleate stages. The RAFTIN1 and TaMS26 genes may contribute to biosynthesis and proper ‘fixation’ of sporopollenin in the development of pollen wall; however, their expression levels were significantly higher at the early tetrad stage and early microspore stage in HT sterile anthers. The recently cloned MS1 gene was expressed at the early tetrad and early microspore stages but not at the trinucleate stage. Moreover, this gene showed extremely significant, high expression in HT sterile anthers compared with normal anthers. These results demonstrate that HT induction of wheat male sterility is probably related to the expression of genes related to carbohydrate metabolism and sporopollenin metabolism. This provides a theoretical basis and technological approach for further studies on the mechanisms of HT induction of male sterility.

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