Abstract:In flowering plants, pollen wall is a specialized extracellular cell-wall matrix surrounding male gametophytes and acts as a natural protector of pollen grains against various environmental and biological stresses. The formation of pollen wall is a complex but well-regulated process, which involves the action of many different genes. However, the genetic and molecular mechanisms underlying this process remain largely unknown.In this study, we isolated and characterized a novel rice male sterile mutant, defecti… Show more
“…Indeed, in pl1, the transcript levels of several key enzyme encoding genes involved in this process were down-regulated ( Figure 8A-D). Consistently, loss-of-function of PL1 decreased the levels of serval waxes components and dominant cutin monomers [52]. These data raise a possibility that PL1 might participate in male development by affecting the metabolic pathway of anther cuticle and pollen exine.…”
Section: Role Of Pl1 In Anther and Pollen Developmentsupporting
confidence: 54%
“…Similar to defective pollen wall 3 (dpw3), another allelic mutant of pl1 (in japonica background) reported very recently [52], our pl1 mutant (in indica background) exhibited slightly swollen tapetum and abnormal primexine matrix formation at stage 9 ( Figures 6H and 7N), and necrosis-like tapetum cell death with less cytoplasmic contents, severely enlarged cell size and compromised cell wall integrity, as well as defective formation of Ubisch bodies and anther cuticle at later stages ( Figure 6L-O and Figure 7P,R,T). However, pl1 had some characteristics distinguished from dpw3.…”
Section: Role Of Pl1 In Anther and Pollen Developmentmentioning
confidence: 62%
“…Together, these results confirmed that the mutation in Os02g01070 is responsible for the defective male-fertility in pl1. In another parallel study, other mutations in Os02g01070, which was named as Defective Pollen Wall 3 (DPW3), were also identified and consistently lead to the similar male-sterile phenotype [52].…”
Section: Int J Mol Sci 2020 21 X For Peer Review 4 Of 21mentioning
Pollen development plays crucial roles in the life cycle of higher plants. Here we characterized a rice mutant with complete male-sterile phenotype, pollen-less 1 (pl1). pl1 exhibited smaller anthers with arrested pollen development, absent Ubisch bodies, necrosis-like tapetal hypertrophy, and smooth anther cuticular surface. Molecular mapping revealed a synonymous mutation in the fourth exon of PL1 co-segregated with the mutant phenotype. This mutation disrupts the exon-intron splice junction in PL1, generating aberrant mRNA species and truncated proteins. PL1 is highly expressed in the tapetal cells of developing anther, and its protein is co-localized with plasma membrane (PM) and endoplasmic reticulum (ER) signal. PL1 encodes an integrin-α FG-GAP repeat-containing protein, which has seven β-sheets and putative Ca2+-binding motifs and is broadly conserved in terrestrial plants. Our findings therefore provide insights into both the role of integrin-α FG-GAP repeat-containing protein in rice male fertility and the influence of exonic mutation on intronic splice donor site selection.
“…Indeed, in pl1, the transcript levels of several key enzyme encoding genes involved in this process were down-regulated ( Figure 8A-D). Consistently, loss-of-function of PL1 decreased the levels of serval waxes components and dominant cutin monomers [52]. These data raise a possibility that PL1 might participate in male development by affecting the metabolic pathway of anther cuticle and pollen exine.…”
Section: Role Of Pl1 In Anther and Pollen Developmentsupporting
confidence: 54%
“…Similar to defective pollen wall 3 (dpw3), another allelic mutant of pl1 (in japonica background) reported very recently [52], our pl1 mutant (in indica background) exhibited slightly swollen tapetum and abnormal primexine matrix formation at stage 9 ( Figures 6H and 7N), and necrosis-like tapetum cell death with less cytoplasmic contents, severely enlarged cell size and compromised cell wall integrity, as well as defective formation of Ubisch bodies and anther cuticle at later stages ( Figure 6L-O and Figure 7P,R,T). However, pl1 had some characteristics distinguished from dpw3.…”
Section: Role Of Pl1 In Anther and Pollen Developmentmentioning
confidence: 62%
“…Together, these results confirmed that the mutation in Os02g01070 is responsible for the defective male-fertility in pl1. In another parallel study, other mutations in Os02g01070, which was named as Defective Pollen Wall 3 (DPW3), were also identified and consistently lead to the similar male-sterile phenotype [52].…”
Section: Int J Mol Sci 2020 21 X For Peer Review 4 Of 21mentioning
Pollen development plays crucial roles in the life cycle of higher plants. Here we characterized a rice mutant with complete male-sterile phenotype, pollen-less 1 (pl1). pl1 exhibited smaller anthers with arrested pollen development, absent Ubisch bodies, necrosis-like tapetal hypertrophy, and smooth anther cuticular surface. Molecular mapping revealed a synonymous mutation in the fourth exon of PL1 co-segregated with the mutant phenotype. This mutation disrupts the exon-intron splice junction in PL1, generating aberrant mRNA species and truncated proteins. PL1 is highly expressed in the tapetal cells of developing anther, and its protein is co-localized with plasma membrane (PM) and endoplasmic reticulum (ER) signal. PL1 encodes an integrin-α FG-GAP repeat-containing protein, which has seven β-sheets and putative Ca2+-binding motifs and is broadly conserved in terrestrial plants. Our findings therefore provide insights into both the role of integrin-α FG-GAP repeat-containing protein in rice male fertility and the influence of exonic mutation on intronic splice donor site selection.
“…The main lipid precursors of sporopollenin include linear fatty acids and monomers of oxygen-containing aromatic compounds, such as coumarin (C9) and ferulic acid (C10), all of which are synthesized in the tapetum cells [26]. In recent years, many genes that are involved in fatty acid metabolism and mediating anther cuticle and sporopollenin formation, whose mutation often leads to male sterile in Arabidopsis thaliana, rice and maize have been reported [19,29,30]. In addition, phospholipase a (releases lysophospholipids) and lipoxygenase (catalyses fatty acid oxidation) were involved in regulating pollen germination in olive (Olea europaea L.) [31].…”
The anther cuticle, which is mainly composed of lipid polymers, functions as physical barriers to protect genetic material intact; however, the mechanism of lipid biosynthesis in maize (Zea mays. L.) anther remains unclear. Herein, we report a male sterile mutant, male sterile 305 (ms305), in maize. It was shown that the mutant displayed a defective anther tapetum development and premature microspore degradation. Three pathways that are associated with the development of male sterile, including phenylpropanoid biosynthesis, biosynthesis of secondary metabolites, as well as cutin, suberine, and wax biosynthesis, were identified by transcriptome analysis. Gas chromatography-mass spectrometry disclosed that the content of cutin in ms305 anther was significantly lower than that of fertile siblings during the abortion stage, so did the total fatty acids, which indicated that ms305 mutation might lead to blocked synthesis of cutin and fatty acids in anther. Lipidome analysis uncovered that the content of phosphatidylcholine, phosphatidylserine, diacylglycerol, monogalactosyldiacylglycerol, and digalactosyldiacylglycerol in ms305 anther was significantly lower when compared with its fertile siblings, which suggested that ms305 mutation disrupted lipid synthesis. In conclusion, our findings indicated that ms305 might affect anther cuticle and microspore development by regulating the temporal progression of the lipidome in maize.
“…However, some evidences demonstrates that carotenoids, avonoids, isoprenoids (terpenoids) and sterol esters are also precursors for the anther cuticle formation [9,10]. Several TTP-speci c genes have been showed to be essential to the early formation of anther cuticle and pollen exine, such as DPW, DPW2, OsGPAT3, DWP3, OsNP1, CYP704B2 and CYP703A3 in rice [11][12][13][14][15][16][17]. In plants, the CER family, also known as the Glossy (GL) family, have been reported to be involve in the accumulation of epicuticular waxes.…”
Background: Male sterility is a simple and efficient pollination control system that is widely exploited in hybrid breeding. In upland cotton, CCRI9106, a photosensitive genetic male sterile (PGMS) mutant isolated from CCRI040029, was reported of great advantages to cotton heterosis. However, little information concerning the male sterility of CCRI9106 is known. Here, comparative transcriptome analysis of CCRI9106 (the mutant, MT) and CCRI040029 (the wild type, WT) anthers in Anyang (long-day, male sterile condition to CCRI9106) was performed to reveal the potential male sterile mechanism of CCRI9106.Results: Light and electron microscopy revealed that the male sterility phenotype of MT was mainly attributed to irregularly exine, lacking tryphine and immature anther cuticle. Based on the cytological characteristics of MT anthers, anther RNA libraries (18 in total) of tetrad (TTP), late uninucleate (LUNP) and binucleate (BNP) stages in MT and WT were constructed for transcriptomic analysis, therefore revealing a total of 870,4 differentially expressed genes (DEGs). By performing gene expression pattern analysis and protein-protein interaction (PPI) networks construction, we found down-regulation of DEGs, which enriched by the lipid biosynthetic process and the synthesis pathways of several types of secondary metabolites such as terpenoids, flavonoids and steroids, may crucial to the male sterility phenotype of MT, and resulting in the defects of anther cuticle and tryphine, even the irregularly exine. Furthermore, several lipid-related genes together with ABA-related genes and MYB transcription factors were identified as hub genes via weighted gene co-expression network analysis (WGCNA). Additionally, the ABA content of MT anthers was reduced across all stages when compared with WT anthers. At last, genes related to the formation of anther cuticle and tryphine could activated in MT under short-day condition.Conclusions: We propose that the down-regulation of genes related to the assembly of anther cuticle and tryphine may lead to the male sterile phenotype of MT, and MYB transcription factors together with ABA played key regulatory roles in these processes. The conversion of fertility in different photoperiods may closely relate to the functional expression of these genes. These findings contribute to elucidate the mechanism of male sterility in upland cotton.
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