scholarly journals AGRONOMIC PERFORMANCE OF MALE-STERILE AND FERTILE

Author(s):  
Georgeta Oroian ◽  
G. Morar ◽  
I. Haş ◽  
Voichiţa Haş

The use of cytoplasmatic male-sterility in maize seed production contributes to increase economical efficiency and to obtain great genetical seeds. Through this theme one has followed the realization of a comparative study between some hybrids obtained to Turda on C and T cytoplasm their homologues, developed with normal and through the castration of the maternal parents. The researches aimed mainly the phenotypic and genotypic variability of the hybrids, the degree of male-sterility and the capacity of production, in phytotechnic conditions in different densities.

Author(s):  
Georgeta Oroian ◽  
G. Morar ◽  
I. Has ◽  
Voichita Has ◽  
Ana Copandean

Cytoplasm male sterility is used for producing hybrid corn seeds by reason of the economic efficiency and is also advantageous for genetic purity of seeds. Three types of male sterility cytoplasm in maize are used as cms maternal parents to produce hybrids: cms-C, cms-S. cms-T. Through this theme one has followed the realization of a comparative study between some hybrids obtained to Turda on C and T cytoplasm their homologues, developed with normal and through the castration of the maternal parents. The researches aimed mainly the phenotypic and genotypic variability of the hybrids, the degree of male-sterility and the capacity of production, in phytotechnic conditions in different densities


2016 ◽  
Vol 113 (49) ◽  
pp. 14145-14150 ◽  
Author(s):  
Zhenyi Chang ◽  
Zhufeng Chen ◽  
Na Wang ◽  
Gang Xie ◽  
Jiawei Lu ◽  
...  

The breeding and large-scale adoption of hybrid seeds is an important achievement in agriculture. Rice hybrid seed production uses cytoplasmic male sterile lines or photoperiod/thermo-sensitive genic male sterile lines (PTGMS) as female parent. Cytoplasmic male sterile lines are propagated via cross-pollination by corresponding maintainer lines, whereas PTGMS lines are propagated via self-pollination under environmental conditions restoring male fertility. Despite huge successes, both systems have their intrinsic drawbacks. Here, we constructed a rice male sterility system using a nuclear gene named Oryza sativa No Pollen 1 (OsNP1). OsNP1 encodes a putative glucose–methanol–choline oxidoreductase regulating tapetum degeneration and pollen exine formation; it is specifically expressed in the tapetum and miscrospores. The osnp1 mutant plant displays normal vegetative growth but complete male sterility insensitive to environmental conditions. OsNP1 was coupled with an α-amylase gene to devitalize transgenic pollen and the red fluorescence protein (DsRed) gene to mark transgenic seed and transformed into the osnp1 mutant. Self-pollination of the transgenic plant carrying a single hemizygous transgene produced nontransgenic male sterile and transgenic fertile seeds in 1:1 ratio that can be sorted out based on the red fluorescence coded by DsRed. Cross-pollination of the fertile transgenic plants to the nontransgenic male sterile plants propagated the male sterile seeds of high purity. The male sterile line was crossed with ∼1,200 individual rice germplasms available. Approximately 85% of the F1s outperformed their parents in per plant yield, and 10% out-yielded the best local cultivars, indicating that the technology is promising in hybrid rice breeding and production.


HortScience ◽  
1990 ◽  
Vol 25 (9) ◽  
pp. 1168e-1168 ◽  
Author(s):  
Edward C. Tigchelaar

The coupling phase linkages have been synthesized between the gene aw (without anthocyanin) and the male sterile gene ms15 (and its alleles ms26, ms47, and an Israeli source of male sterility). Less than 2 map units separate aw and ms15 on chromosome 2, providing a convenient seedling marker gene to rapidly identify male sterility for both inbred development and hybrid seed production. The seedling marker also provides a convenient marker to rapidly assess hybrid seed purity. Unique features of each of the alleles involved in male sterility and their use in inbred and hybrid development will be described.


1990 ◽  
Vol 70 (3) ◽  
pp. 611-618 ◽  
Author(s):  
R. PINNISCH ◽  
P. B. E. McVETTY

Hybrid summer rape (Brassica napus L.) seed production blocks were established at two locations in Manitoba in 1986 and 1987 to examine the effect of distance from the pollen source on seed yield, (both total and hybrid) and percent hybridity of seed produced on rows of a male sterile line of the open pollinated population B. napus cultivar, Marnoo, possessing the pol cytoplasmic male sterility inducing cytoplasm. A 10:1 ratio of male sterile line (A-line) to pollen parent was employed. Leaf cutter bees (Megachile rotundata F.) were used as the pollen vector between the two parents. In 1986, no significant differences in total seed yield were found among A-line rows, while in 1987, significant differences in total seed yields of A-line rows were found. Differences in hybrid seed yields among A-line rows were significant for all locations and years. Leaf cutter bees were found to be effective pollinators of the A-line plants. Less than half and less than a third of the seed produced on the A-line rows in 1986 and 1987, respectively, was hybrid seed. The high percentage of non-hybrid seed present in the seed lot may have been due to incomplete male sterility of the Marnoo A-line population. Total seed yields, hybrid seed yields and percent hybridity all declined linearly as distance from the pollen source increased. Improvement in the degree of male sterility of the Marnoo A-line population and/or a reduction in the 10:1 ratio of parents, and subsequent maximum A-line row to R-line row distance, will be necessary if hybrid summer rape seed production using this pol CMS A-line is to be commercially viable.Key words: Brassica napus L., CMS, hybrid, hybridity


2004 ◽  
Vol 129 (6) ◽  
pp. 819-825 ◽  
Author(s):  
Soon O. Park ◽  
Kevin M. Crosby ◽  
Rongfeng Huang ◽  
T. Erik Mirkov

Male sterility is an important trait of melon in F1 hybrid seed production. Molecular markers linked to a male-sterile gene would be useful in transferring male sterility into fertile melon cultivars and breeding lines. However, markers linked to the ms-3 gene for male sterility present in melon have not been reported. Our objectives were to identify randomly amplified polymorphic DNA (RAPD) markers linked to the ms-3 gene controlling male sterility using bulked segregant analysis in an F2 population from the melon cross of line ms-3 (male-sterile) × `TAM Dulce' (male-fertile), convert the most tightly linked RAPD marker to the ms-3 gene into a sequence characterized amplified region (SCAR) marker based on a specific forward and reverse 20-mer primer pair, and confirm the linkage of the RAPD and SCAR markers with the ms-3 gene in an F2 population from the cross of line ms-3 × `Mission' (male-fertile). A single recessive gene controlling male sterility was found in F2 individuals and confirmed in F3 families. Two RAPD markers that displayed an amplified DNA fragment in the male-sterile bulk were detected to be linked to the ms-3 gene in the F2 population from the cross of line ms-3 × `TAM Dulce'. RAPD marker OAM08.650 was closely linked to the ms-3 gene at 2.1 cM. SCAR marker SOAM08.644 was developed on the basis of the specific primer pair designed from the sequence of the RAPD marker OAM08.650. The linked RAPD and SCAR markers were confirmed in the F2 population from the cross of line ms-3 × `Mission' to be consistently linked to the ms-3 gene at 5.2 cM. These markers were also present in 22 heterozygous fertile F1 plants having the ms-3 gene. The RAPD and SCAR markers linked to the ms-3 gene identified, and confirmed here could be utilized for backcrossing of male sterility into elite melon cultivars and lines for use as parents for F1 hybrid seed production.


2021 ◽  
Vol 22 (12) ◽  
pp. 6388
Author(s):  
Miaomiao Hao ◽  
Wenlong Yang ◽  
Weiwen Lu ◽  
Linhe Sun ◽  
Muhammad Shoaib ◽  
...  

Heterosis utilization is very important in hybrid seed production. An AL-type cytoplasmic male sterile (CMS) line has been used in wheat-hybrid seed production, but its sterility mechanism has not been explored. In the present study, we sequenced and verified the candidate CMS gene in the AL-type sterile line (AL18A) and its maintainer line (AL18B). In the late uni-nucleate stage, the tapetum cells of AL18A showed delayed programmed cell death (PCD) and termination of microspore at the bi-nucleate stage. As compared to AL18B, the AL18A line produced 100% aborted pollens. The mitochondrial genomes of AL18A and AL18B were sequenced using the next generation sequencing such as Hiseq and PacBio. It was found that the mitochondrial genome of AL18A had 99% similarity with that of Triticum timopheevii, AL18B was identical to that of Triticum aestivum cv. Chinese Yumai. Based on transmembrane structure prediction, 12 orfs were selected as candidate CMS genes, including a previously suggested orf256. Only the lines harboring orf279 showed sterility in the transgenic Arabidopsis system, indicating that orf279 is the CMS gene in the AL-type wheat CMS lines. These results provide a theoretical basis and data support to further analyze the mechanism of AL-type cytoplasmic male sterility in wheat.


2019 ◽  
Vol 40 (04) ◽  
Author(s):  
Pramod Sharma ◽  
Sunil A Nair ◽  
Payal Sharma

Male sterility is described as absence of functional pollen grains in hermaphrodite flowers facilitating large scale production of hybrid seeds in vegetable crops. It eases hybrid seed production at commercial level in crops like tomato, chilli, capsicum, carrot, onion, cabbage, cauliflower and cucurbits. Male sterility would reduce the cost of hybrid seed production by limiting the labour making it efficient and economical. Incorporation of biotechnological tools in conventional plant breeding techniques would aid the breeders in limiting the drawbacks surrounding exploitation of male sterility for development of new hybrids. The present review is an attempt to summarize and to know the commercial utilization of male sterile line in hybrid seed production of vegetables.


2021 ◽  
Vol 12 ◽  
Author(s):  
Wei Dong ◽  
Dewei Wu ◽  
Chen Yan ◽  
Defeng Wu

Seed production is critical for watermelon production, which mostly involves first-generation hybrid varieties. However, watermelon hybrid seed production currently requires complex procedures, including artificial isolation and pollination. Therefore, the development and use of a male-sterile system to generate watermelon hybrids can simplify the process. The scarcity of male-sterile watermelon germplasm resources necessitates the use of molecular breeding methods. Unfortunately, the genes responsible for male sterility in watermelon have not been cloned. Thus, the genetic basis of the male sterility remains unknown. In this study, two DNA pools derived from male-sterile and normal plants in the F2 population were used for whole-genome resequencing. The Illumina high-throughput sequencing resulted in 62.99 Gbp clean reads, with a Q30 of 80% after filtering. On the basis of the SNP index association algorithm, eight candidate regions (0.32 Mb) related to specific traits were detected on chromosome 6. Expression pattern analyses and watermelon transformation studies generated preliminary evidence that Cla006625 encodes a pollen-specific leucine-rich repeat protein (ClaPEX1) influencing the male sterility of watermelon. The identification and use of genic male sterility genes will promote watermelon male sterility research and lay the foundation for the efficient application of seed production technology.


HortScience ◽  
1996 ◽  
Vol 31 (1) ◽  
pp. 123-126 ◽  
Author(s):  
X.P. Zhang ◽  
B.B. Rhodes ◽  
W.V. Baird ◽  
H.T. Skorupska ◽  
W.C. Bridges

Hybrid seed production can be facilitated by using male sterility coupled with a seedling marker. This research was initiated to combine the ms male sterility and dg delayed-green seedling marker into watermelon [Citrullus lanatus (Thunb.) Matsum. & Nakai] lines. Male-sterile plants of the male-sterile line G17AB were crossed with plants of delayed-green breeding line Pale90, which has yellow cotyledons and pale-green, newly developed, true leaves. The double-recessive recombinants, male sterile and delayed green, from the F2 population were backcrossed to the male-fertile plants of G17AB. The pedigree method was used for selection in the progenies. The segregation ratios obtained from F2 and BC1F2 populations suggest that the male-sterile and delayed-green traits are inherited independently and that delayed green is inherited as a single recessive nuclear gene. Two male-sterile watermelon lines with delayed-green seedling marker have been developed. These lines will provide a convenient way to introduce male sterility and the delayed-green seedling marker into various genetic backgrounds. These two lines can be used for testing the efficiency of a new, hybrid, watermelon, seed production system.


Author(s):  
Junping Yu ◽  
Guolong Zhao ◽  
Wei Li ◽  
Ying Zhang ◽  
Peng Wang ◽  
...  

Abstract Key message Identification and functional analysis of the male sterile gene MS6 in Glycine max. Abstract Soybean (Glycine max (L.) Merr.) is an important crop providing vegetable oil and protein. The male sterility-based hybrid breeding is a promising method for improving soybean yield to meet the globally growing demand. In this research, we identified a soybean genic male sterile locus, MS6, by combining the bulked segregant analysis sequencing method and the map-based cloning technology. MS6, highly expressed in anther, encodes an R2R3 MYB transcription factor (GmTDF1-1) that is homologous to Tapetal Development and Function 1, a key factor for anther development in Arabidopsis and rice. In male sterile ms6 (Ames1), the mutant allele contains a missense mutation, leading to the 76th leucine substituted by histidine in the DNA binding domain of GmTDF1-1. The expression of soybean MS6 under the control of the AtTDF1 promoter could rescue the male sterility of attdf1 but ms6 could not. Additionally, ms6 overexpression in wild-type Arabidopsis did not affect anther development. These results evidence that GmTDF1-1 is a functional TDF1 homolog and L76H disrupts its function. Notably, GmTDF1-1 shows 92% sequence identity with another soybean protein termed as GmTDF1-2, whose active expression also restored the fertility of attdf1. However, GmTDF1-2 is constitutively expressed at a very low level in soybean, and therefore, not able to compensate for the MS6 deficiency. Analysis of the TDF1-involved anther development regulatory pathway showed that expressions of the genes downstream of TDF1 are significantly suppressed in ms6, unveiling that GmTDF1-1 is a core transcription factor regulating soybean anther development.


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