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• W2016186178 abstract "Abstract Background In plants, pollination is a critical step in reproduction. During pollination, constant communication between male pollen and the female stigma is required for pollen adhesion, germination, and tube growth. The detailed mechanisms of stigma-mediated reproductive processes, however, remain largely unknown. Maize ( Zea mays L.), one of the world’s most important crops, has been extensively used as a model species to study molecular mechanisms of pollen and stigma interaction. A comprehensive analysis of maize silk transcriptome may provide valuable information for investigating stigma functionality. A comparative analysis of expression profiles between maize silk and dry stigmas of other species might reveal conserved and diverse mechanisms that underlie stigma-mediated reproductive processes in various plant species. Results Transcript abundance profiles of mature silk, mature pollen, mature ovary, and seedling were investigated using RNA-seq. By comparing the transcriptomes of these tissues, we identified 1,427 genes specifically or preferentially expressed in maize silk. Bioinformatic analyses of these genes revealed many genes with known functions in plant reproduction as well as novel candidate genes that encode amino acid transporters, peptide and oligopeptide transporters, and cysteine-rich receptor-like kinases. In addition, comparison of gene sets specifically or preferentially expressed in stigmas of maize, rice ( Oryza sativa L.), and Arabidopsis ( Arabidopsis thaliana [L.] Heynh.) identified a number of homologous genes involved either in pollen adhesion, hydration, and germination or in initial growth and penetration of pollen tubes into the stigma surface. The comparison also indicated that maize shares a more similar profile and larger number of conserved genes with rice than with Arabidopsis, and that amino acid and lipid transport-related genes are distinctively overrepresented in maize. Conclusions Many of the novel genes uncovered in this study are potentially involved in stigma-mediated reproductive processes, including genes encoding amino acid transporters, peptide and oligopeptide transporters, and cysteine-rich receptor-like kinases. The data also suggest that dry stigmas share similar mechanisms at early stages of pollen-stigma interaction. Compared with Arabidopsis, maize and rice appear to have more conserved functional mechanisms. Genes involved in amino acid and lipid transport may be responsible for mechanisms in the reproductive process that are unique to maize silk." @default.
• W2016186178 created "2016-06-24" @default.
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• W2016186178 date "2012-07-02" @default.
• W2016186178 modified "2023-10-12" @default.
• W2016186178 title "Identification of genes specifically or preferentially expressed in maize silk reveals similarity and diversity in transcript abundance of different dry stigmas" @default.
• W2016186178 cites W1491616831 @default.
• W2016186178 cites W1576499916 @default.
• W2016186178 cites W1798932742 @default.
• W2016186178 cites W1890820161 @default.
• W2016186178 cites W1966225891 @default.
• W2016186178 cites W1970817498 @default.
• W2016186178 cites W1975486814 @default.
• W2016186178 cites W1977543378 @default.
• W2016186178 cites W1978986148 @default.
• W2016186178 cites W1981509058 @default.
• W2016186178 cites W1986662234 @default.
• W2016186178 cites W1991479491 @default.
• W2016186178 cites W1992512552 @default.
• W2016186178 cites W1992710932 @default.
• W2016186178 cites W2001897837 @default.
• W2016186178 cites W2005105507 @default.
• W2016186178 cites W2005297100 @default.
• W2016186178 cites W2015643257 @default.
• W2016186178 cites W2017958516 @default.
• W2016186178 cites W2023001306 @default.
• W2016186178 cites W2024593543 @default.
• W2016186178 cites W2030924578 @default.
• W2016186178 cites W2039229026 @default.
• W2016186178 cites W2042230973 @default.
• W2016186178 cites W2047339015 @default.
• W2016186178 cites W2053633817 @default.
• W2016186178 cites W2054110282 @default.
• W2016186178 cites W2056206951 @default.
• W2016186178 cites W2057271763 @default.
• W2016186178 cites W2057794854 @default.
• W2016186178 cites W2059855917 @default.
• W2016186178 cites W2069102911 @default.
• W2016186178 cites W2074301394 @default.
• W2016186178 cites W2076513999 @default.
• W2016186178 cites W2080304795 @default.
• W2016186178 cites W2084669999 @default.
• W2016186178 cites W2087703982 @default.
• W2016186178 cites W2089359989 @default.
• W2016186178 cites W2092806862 @default.
• W2016186178 cites W2094580636 @default.
• W2016186178 cites W2096416412 @default.
• W2016186178 cites W2097341408 @default.
• W2016186178 cites W2099091088 @default.
• W2016186178 cites W2100609602 @default.
• W2016186178 cites W2103196178 @default.
• W2016186178 cites W2103821115 @default.
• W2016186178 cites W2104012706 @default.
• W2016186178 cites W2104408556 @default.
• W2016186178 cites W2109428210 @default.
• W2016186178 cites W2110480573 @default.
• W2016186178 cites W2113216487 @default.
• W2016186178 cites W2114728372 @default.
• W2016186178 cites W2118316417 @default.
• W2016186178 cites W2120237563 @default.
• W2016186178 cites W2125490697 @default.
• W2016186178 cites W2130038001 @default.
• W2016186178 cites W2130581883 @default.
• W2016186178 cites W2141502826 @default.
• W2016186178 cites W2146516445 @default.
• W2016186178 cites W2147186621 @default.
• W2016186178 cites W2148468309 @default.
• W2016186178 cites W2150863418 @default.
• W2016186178 cites W2150871890 @default.
• W2016186178 cites W2150995168 @default.
• W2016186178 cites W2153731402 @default.
• W2016186178 cites W2154431984 @default.
• W2016186178 cites W2158485283 @default.
• W2016186178 cites W2159690786 @default.
• W2016186178 cites W2159860789 @default.
• W2016186178 cites W2163713467 @default.
• W2016186178 cites W2163714044 @default.
• W2016186178 cites W2163800448 @default.
• W2016186178 cites W2167760722 @default.
• W2016186178 cites W2170989872 @default.
• W2016186178 cites W2276004791 @default.
• W2016186178 cites W257724043 @default.
• W2016186178 cites W306229212 @default.
• W2016186178 cites W4294107304 @default.
• W2016186178 doi "https://doi.org/10.1186/1471-2164-13-294" @default.
• W2016186178 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3416702" @default.
• W2016186178 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/22748054" @default.
• W2016186178 hasPublicationYear "2012" @default.
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