scholarly journals Identification of fertility-related genes for maize CMS-S via Bulked Segregant RNA-Seq

PeerJ ◽  
2020 ◽  
Vol 8 ◽  
pp. e10015
Author(s):  
Xiner Qin ◽  
Wenliang Zhang ◽  
Xue Dong ◽  
Shike Tian ◽  
Panpan Zhang ◽  
...  

Cytoplasmic male sterility (CMS) is extensively used in maize hybrid production, and identification of genes related to fertility restoration for CMS is important for hybrid breeding. The fertility restoration of S type CMS is governed by several loci with major and minor effects, while the mechanism of fertility restoration for CMS-S is still unknown. In this study, BSR-Seq was conducted with two backcrossing populations with the fertility restoration genes, Rf3 and Rf10, respectively. Genetic mapping via BSR-Seq verified the positions of the two loci. A total of 353 and 176 differentially expressed genes (DEGs) between the male fertility and male sterile pools were identified in the populations with Rf3 and Rf10, respectively. In total, 265 DEGs were co-expressed in the two populations, which were up-regulated in the fertile plants, and they might be related to male fertility involving in anther or pollen development. Moreover, 35 and seven DEGs were specifically up-regulated in the fertile plants of the population with Rf3 and Rf10, respectively. Function analysis of these DEGs revealed that jasmonic acid (JA) signal pathway might be involved in the Rf3 mediated fertility restoration for CMS-S, while the small ubiquitin-related modifier system could play a role in the fertility restoration of Rf10.

2021 ◽  
Author(s):  
Nari Yu ◽  
Sunggil Kim

Abstract Cytoplasmic male-sterility (CMS) has been exclusively used to produce F1 hybrid seeds of onion (Allium cepa L.). A single nuclear locus, Ms, is known to restore male-fertility of CMS in onions. Unstable male-sterile onions producing a small amount of pollen grains have been identified in a previous study. When such unstable male-sterile onions were crossed with stable male-sterile onions containing CMS-T cytoplasm, male-fertility was completely restored, although genotypes of the Ms locus were homozygous recessive. Inheritance patterns indicated that male-fertility restoration was controlled by a single locus designated as Ms2. A combined approach of bulked segregant analysis and RNA-seq was used to identify candidate genes for the Ms2 locus. High resolution melting (HRM) markers were developed based on single nucleotide polymorphisms (SNPs) detected by RNA-Seq. Comparative mapping of the Ms2 locus showed that Ms2 was positioned at the end of chromosome 2 with a distance of approximately 70 cM away from the Ms locus. Although 38 contigs containing reliable SNPs were analyzed using recombinants selected from 1,344 individuals, no contig showed perfect linkage to Ms2. Interestingly, transcription levels of orf725, a CMS-associated gene in onions, were significantly reduced in male-fertile individuals of segregating populations. However, no significant change in its transcription level was observed in individuals of a segregating population with male-fertility phenotypes determined by the Ms locus, suggesting that male-fertility restoration mechanism of Ms2 might be different from that of the Ms locus.


Genetics ◽  
1997 ◽  
Vol 147 (3) ◽  
pp. 1317-1328
Author(s):  
Anita A de Haan ◽  
Hans P Koelewijn ◽  
Maria P J Hundscheid ◽  
Jos M M Van Damme

Male fertility in Plantago lanceolata is controlled by the interaction of cytoplasmic and nuclear genes. Different cytoplasmic male sterility (CMS) types can be either male sterile or hermaphrodite, depending on the presence of nuclear restorer alleles. In three CMS types of P. lanceolata (CMSI, CMSIIa, and CMSIIb) the number of loci involved in male fertility restoration was determined. In each CMS type, male fertility was restored by multiple genes with either dominant or recessive action and capable either of restoring male fertility independently or in interaction with each other (epistasis). Restorer allele frequencies for CMSI, CMSIIa and CMSIIb were determined by crossing hermaphrodites with “standard” male steriles. Segregation of male steriles vs. non-male steriles was used to estimate overall restorer allele frequency. The frequency of restorer alleles was different for the CMS types: restorer alleles for CMSI were less frequent than for CMSIIa and CMSIIb. On the basis of the frequencies of male steriles and the CMS types an “expected” restorer allele frequency could be calculated. The correlation between estimated and expected restorer allele frequency was significant.


2020 ◽  
Vol 61 (5) ◽  
pp. 988-1004 ◽  
Author(s):  
Xiaoying Pan ◽  
Wei Yan ◽  
Zhenyi Chang ◽  
Yingchao Xu ◽  
Ming Luo ◽  
...  

Abstract Pollen development is critical to the reproductive success of flowering plants, but how it is regulated is not well understood. Here, we isolated two allelic male-sterile mutants of OsMYB80 and investigated how OsMYB80 regulates male fertility in rice. OsMYB80 was barely expressed in tissues other than anthers, where it initiated the expression during meiosis, reached the peak at the tetrad-releasing stage and then quickly declined afterward. The osmyb80 mutants exhibited premature tapetum cell death, lack of Ubisch bodies, no exine and microspore degeneration. To understand how OsMYB80 regulates anther development, RNA-seq analysis was conducted to identify genes differentially regulated by OsMYB80 in rice anthers. In addition, DNA affinity purification sequencing (DAP-seq) analysis was performed to identify DNA fragments interacting with OsMYB80 in vitro. Overlap of the genes identified by RNA-seq and DAP-seq revealed 188 genes that were differentially regulated by OsMYB80 and also carried an OsMYB80-interacting DNA element in the promoter. Ten of these promoter elements were randomly selected for gel shift assay and yeast one-hybrid assay, and all showed OsMYB80 binding. The 10 promoters also showed OsMYB80-dependent induction when co-expressed in rice protoplast. Functional annotation of the 188 genes suggested that OsMYB80 regulates male fertility by directly targeting multiple biological processes. The identification of these genes significantly enriched the gene networks governing anther development and provided much new information for the understanding of pollen development and male fertility.


2007 ◽  
Vol 126 (3) ◽  
pp. 302-305 ◽  
Author(s):  
S. P. Yang ◽  
M. P. Duan ◽  
Q. C. Meng ◽  
J. Qiu ◽  
J. M. Fan ◽  
...  

2019 ◽  
Author(s):  
Jiali Ye ◽  
Xuetong Yang ◽  
Zhiquan Yang ◽  
Wei Li ◽  
Qi Liu ◽  
...  

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.


2016 ◽  
Vol 8 (2) ◽  
pp. 10
Author(s):  
Konstantinos S. Krommydas ◽  
Zisis Tzikalios ◽  
Panagiotis Madesis ◽  
Fotios A. Bletsos ◽  
Athanasios Mavromatis ◽  
...  

<p>A functional cytoplasmic male sterile (CMS) eggplant line carrying the cytoplasm of <em>Solanum violaceum</em> was developed in the past, but the fertility restoring genes (<em>Rf</em>-genes) were not identified. This work aimed to produce the CMS lines of three Hellenic eggplant cultivars (viz., ‘Langada’, ‘Emi’ and ‘Tsakoniki’) using the cytoplasm of <em>S. violaceum</em> and study the inheritance of the <em>Rf</em>-genes. The respective CMS eggplant lines were developed by the backcross method and examined for their fertility parameters. The results demonstrated that female fertility was not affected by the cytoplasm of <em>S. violaceum</em>. In contrast, the occurrence of three male fertility phenotypes (male sterile, male fertile and potentially male fertile) indicated that male fertility was affected by nuclear/cytoplasmic interactions. Male sterile plants were characterized by indehiscent anthers, low pollen viability and abnormal anther morphology. Male fertile plants formed dehiscent anthers with high pollen viability and normal morphology. Potentially male fertile plants initially formed dehiscent anthers, but in later stages formed exclusively indehiscent anthers. Male fertile plants were obtained in the advanced backcross populations of CMS ‘Tsakoniki’, but not in CMS ‘Langada’ and CMS ‘Emi’. The genetic analysis of fertility restoration indicated that male fertility in the genetic background of cv. ‘Tsakoniki’ is controlled by one essential genetic locus, affected by a secondary modifying locus. Molecular analysis of cp-DNA and mt-DNA in the CMS lines indicated maternal inheritance of the cytoplasm organelles. Our findings demonstrate that the genotype of the eggplant parent can affect the expression of CMS as well as fertility restoration.</p>


Genetics ◽  
1982 ◽  
Vol 102 (2) ◽  
pp. 285-295
Author(s):  
H Ahokas

ABSTRACT A new cytoplasmic male sterility in barley (Hordeum vulgare s.l.) is described and designated as msm2. The cytoplasm was derived from a selection of the wild progenitor of barley (H. vulgare ssp. spontaneum). This selection, 79BS14-3, originates from the Southern Coastal Plain of Israel. The selection 79BS14-3 has a normal spike fertility in Finland. When 79BS14-3 was crossed by cv. Adorra, the F1 displayed partial male fertility and progeny of recurrent backcrosses with cv. Adorra were completely male sterile. Evidently 79BS14-3 is a carrier of a recessive or semidominant restorer gene of fertility. The dominant restorer gene Rfm1a for another cytoplasmic male sterility, msm1, is also effective in msm2 cytoplasm. The different partial fertility restoration properties of msm2 and msm1 cause these cytoplasms to be regarded as being distinct. Seventy spontaneum accessions from Israel have been studied for their capacity to produce F1 restoration of male fertility both in msm1 and in msm2 cytoplasms with a cv. Adorra-like seed parent (nuclear gene) background. The msm2 cytoplasm shows partial restoration more commonly than msm1 in these F1 combinations. The mean restoration percentage per accession for msm2 is 28, and for msm1 4. Most of the F1 seed set differences of the two cytoplasms are statistically significant. When estimated with partially restored F1 combinations, msm2 cytoplasm appeared to be about 50 times more sensitive to the male fertility-promoting genes present in the spontaneum accessions. The spontaneum sample from Central and Western Negev, which has been found to be devoid of restoration ability in msm1 cytoplasm, had only low partial restoration ability in msm2 (mean 0.3%). The female fertility of msm2 appears normal. The new msm2 cytoplasm could be useful in producing hybrid barley.


2010 ◽  
Vol 135 (1) ◽  
pp. 49-52 ◽  
Author(s):  
Sergio Melgar ◽  
Michael J. Havey

The most commonly used source of cytoplasmic male sterility in onion (Allium cepa) is controlled by the interaction of the cytoplasm [male-sterile (S) or normal male-fertile (N)] and one nuclear male-fertility-restoration locus (Ms). Scoring of genotypes at Ms is generally done by testcrossing male-fertile to male-sterile (S msms) plants, followed by scoring of testcross progenies for male-fertility restoration. We identified two N-cytoplasmic families, one that was homozygous dominant and the other segregating at Ms. Plants from each of these two families were individually testcrossed to male-sterile onion. Nuclear restoration of male fertility in testcross progenies was evaluated in the field over 4 years. For male plants homozygous dominant at Ms, we expected testcross families to show 100% male-fertility restoration, but observed mean values between 46% and 100%. For plants segregating at Ms, we again observed lower than expected frequencies of male-fertility restoration. These results demonstrate that the dominant Ms allele shows reduced penetrance, requiring that male-fertility restoration be scored over years to more confidently assign genotypes at Ms.


HortScience ◽  
1996 ◽  
Vol 31 (4) ◽  
pp. 596c-596
Author(s):  
Yutaka Sato ◽  
Michael J. Havey

The production of hybrid-onion seed depends on cytoplasmic male sterility (CMS) systems. The male-sterile line is seed propagated using a normal (N) cytoplasmic maintainer line homozygous recessive at the nuclear male-fertility restoration locus (MS). Because of onion's biennial generation time, 4 to 8 years are required to establish the genotype at the MS locus. The development of maintainer lines would benefit greatly from a genetic marker linked to the MS locus. Such a marker would allow breeders to establish the nuclear genotype in seedlings and flower only those plants that are maintainers (N msms) or plants that can be used to develop maintainers (N MSms), reducing the number of plants to be testcrossed or backcrossed to a sterile line. We evaluated restriction fragment length polymorphisms (RFLPs), random amplification of polymorphic DNA (RAPDs), and amplified fragment length polymorphisms (AFLPs) to tag the chromosome region carrying the MS locus. No RAPDs or RFLPs cosegregated with MS. AFLP markers were identified that phenotypically correlated with restoration of male fertility.


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