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Maize (Zea mays) represents one of the most successful uses of heterosis among crops. Hybrid maize seeds can be produced by crossing a male-sterile female parent with a male parent as the pollen donor to achieve high seed purity at low cost. Cytoplasmic male sterility (CMS) has been widely used for maize hybrid seed production. Recently, several hybrid seed production technologies based on genic male sterility (GMS) genes have been developed. In addition, the identification of environment-sensitive genic male sterility (EGMS) genes provides opportunities for the two-line system to be applied in maize hybrid seed production. In this review, we systematically summarize the male-sterile genes and molecular mechanisms of male sterility in maize. Future prospects for the study of maize male sterility are highlighted. Future research will enhance our understanding of the molecular regulatory networks of male sterility and promote the process of maize hybrid seed production using male sterile lines. [ABSTRACT FROM AUTHOR]

Rice (Oryza sativa L.) is one of the most important food crops worldwide. The utilisation of heterosis (hybrid vigour) has played a significant role in increasing rice yield and ensuring food supply. Over the past 50 years, the first-generation three-line system based on cytoplasmic male sterility, and the second-generation two-line system based on environment-sensitive genic male sterility (EGMS), have been widely applied in hybrid rice production. However, the three-line system is restricted by the matching relationship among the three parental lines and allows only ~ 2–5% of germplasms to be explored for elite combinations. The environmental sensitivity of EGMS lines has posed serious risks to the production of hybrid seeds. These factors have hindered the development and applications of hybrid rice. Third-generation hybrid rice technology (TGHRT) is based on environment-insensitive genic male sterility, which can effectively overcome the intrinsic problems of the three-line and two-line systems. Since the establishment of TGHRT, numerous findings and innovations have been reported. This paper gives a brief review of traditional hybrid rice technologies and discusses the establishment of TGHRT, technical innovations in TGHRT, and future research that is necessary to promote the wide application of TGHRT in rice production. [ABSTRACT FROM AUTHOR]

Oilseed rape ( OSR; Brassica napus L.) is a major crop in temperate regions and provides an important source of nutrition to many of the yield-enhancing insect flower visitors that consume floral nectar. The manipulation of mechanisms that control various crop plant traits for the benefit of pollinators has been suggested in the bid to increase food security, but little is known about inherent floral trait expression in contemporary OSR varieties or the breeding systems used in OSR breeding programmes. We studied a range of floral traits in glasshouse-grown, certified conventional varieties of winter OSR to test for variation among and within breeding systems. We measured 24-h nectar secretion rate, amount, concentration and ratio of nectar sugars per flower, and sizes and number of flowers produced per plant from 24 varieties of OSR representing open-pollinated ( OP), genic male sterility ( GMS) hybrid and cytoplasmic male sterility ( CMS) hybrid breeding systems. Sugar concentration was consistent among and within the breeding systems; however, GMS hybrids produced more nectar and more sugar per flower than CMS hybrid or OP varieties. With the exception of ratio of fructose/glucose in OP varieties, we found that nectar traits were consistent within all the breeding systems. When scaled, GMS hybrids produced 1.73 times more nectar resource per plant than OP varieties. Nectar production and amount of nectar sugar in OSR plants were independent of number and size of flowers. Our data show that floral traits of glasshouse-grown OSR differed among breeding systems, suggesting that manipulation and enhancement of nectar rewards for insect flower visitors, including pollinators, could be included in future OSR breeding programmes. [ABSTRACT FROM AUTHOR]

In plants, male sterility can be caused either by mitochondrial genes with coupled nuclear genes or by nuclear genes alone; the resulting conditions are known as cytoplasmic male sterility (CMS) and genic male sterility (GMS), respectively. CMS and GMS facilitate hybrid seed production for many crops and thus allow breeders to harness yield gains associated with hybrid vigor (heterosis). In CMS, layers of interaction between mitochondrial and nuclear genes control its male specificity, occurrence, and restoration of fertility. Environment-sensitive GMS (EGMS) mutants may involve epigenetic control by noncoding RNAs and can revert to fertility under different growth conditions, making them useful breeding materials in the hybrid seed industry. Here, we review recent research on CMS and EGMS systems in crops, summarize general models of male sterility and fertility restoration, and discuss the evolutionary significance of these reproductive systems. [ABSTRACT FROM AUTHOR]

Hot pepper is an important vegetable crop of tropics and sub tropics regions of the world. The pungency, red colour and oleoresin contents are important characters in the crop. There are different types of hot pepper are available in the market depending upon the market needs and consumer preference. The genic and cytoplasmic male sterility is available in the crop. Genetic resistance to several diseases and insects pest is also available. Hybrid seed production requires lot of care and intensive supervision. The pollination control mechanisms available are helpful in making the commercial hybrid seed production profitable. [ABSTRACT FROM PUBLISHER]

Limitation in mitochondrial genome diversity of leek, revealed by restriction fragment length polymorphism (RFLP) analyses with mitochondrial gene probes, prevent a cytoplasmic male sterility (CMS) system in elite populations. However, mitochondrial genome diversity was detected in Allium ampeloprasum L. wild accession and landraces, as well as in pearl onion. Within this plant material, nine mitotypes were distinguished and could be used in order to broaden the genetic basis of leek. A chimeric mitochondrial gene configuration is usable as a marker for the sterility inducing cytoplasms (S1) in chives (Allium schoenoprasum L.) and in onion (Allium cepa L.) for (S) and (T) cytoplasm. This chimeric mitochondrial gene configuration is also present in the subgenus Allium, revealed by polymerase chain reaction (PCR). However, only a faint amplicon was observed in a few accessions investigated herein, suggesting that this fragment might be present to a lesser level in mitochondrial DNA, as a sublimon. [ABSTRACT FROM AUTHOR]

Spontaneous mutations leading to male sterility have been described for many different crops and are of great importance to hybrid breeding, provided that their inheritance is resolved. This paper describes an efficient method to characterise male sterilities with respect to cytoplasmic factors that might be causally related to them. The differentiation of cytoplasmic (CMS) and genic (GMS) male sterility is achieved by a specific transfer of nuclear male sterility factors to different cytoplasm types which have previously been distinguished by means of RFLP analyses using mitochondrial gene probes. The nuclear sterility factors of Allium schoenoprasum used, st1 and st2, showed a monogenic recessive inheritance in their original cytoplasms. While st1 was expressed in four different cytoplasm types, st2 did not show itself in a cytoplasm type differing from the original. Therefore, the st1-sterility is a GMS, while a cytoplasmic factor is necessary for the occurrence of st2-sterility. This cytoplasmic factor was verified by a reciprocal cross, and the CMS system was completed by the selection of maintainer genotypes. Neither of these new sterilities were influenced by high temperatures or tetracycline. The benefits of a new CMS system to practical breeding and the advantages and disadvantages of the environmental influences on the expression of male sterility are discussed. [ABSTRACT FROM AUTHOR]