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  • 1
    ISSN: 1432-2145
    Keywords: Maize ; Retrotransposon ; Microspore expression ; Polygalacturonase genes ; Genome structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract We have isolated, by screening a genomic library, a retroelement from maize designated PREM-2 (pollen retroelement maize-2), which is expressed in a tissue-specific manner. RNA transcripts of the PREM-2 family are found in the microspore but not in more mature pollen or in any of the vegetative tissues examined. The expression of PREM-2 elements in the uninucleate microspore provides an explanation for the genetic transmission of genomic rearrangements caused by the transposition of retroelements. PREM-2 elements are very abundant and are estimated to constitute about 5% of the maize genome and could possibly have played an important role in the determination of genome structure and in the generation of repetitive sequences in maize. The entire PREM-2 element is 9439 by long. The LTRs of PREM-2 are 1307 by in length. The internal region between the 5′ and 3′ LTRs contains 6825 by and shares homology to the gag, pro, int, RT, and RNaseH regions of copia-type retroelements. PREM-2 elements have been found in close proximity with several maize genes registered in GenBank. The presence of PREM-2 sequence in the exact 5' flanking position of three polygalacturonase genes expressed in pollen, has been used to examine the evolution of the polygalacturonase multigene family in maize and to estimate the time of the PREM-2 integration event.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1617-4623
    Keywords: Maize ; Pollen development ; Tobacco ; Promoter ; β-Glucuronidase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary A set of 5′ promoter deletions from Zmgl3, a genomic clone of a pollen-specific gene of maize, has been transcriptionally fused to a β-glucuronidase (GUS) reporter gene in the binary vector pBI101. Tobacco leaf disks were transformed and mature plants analyzed for GUS activity directed by the Zmg13 promoter constructs. Transgenic plants containing the 375 by Zmg13 sequence from −314 to +61 relative to the transcription start site transcribed GUS RNA and expressed active GUS enzyme in mature pollen but not in leaves. Plants transformed with a 35S CaMV promoter-GUS transcriptional fusion expressed GUS RNA in leaves but not in pollen. Neither GUS RNA or active enzyme could be detected in pollen or leaves from plants containing a 124 by Zmg13-GUS transcriptional fusion missing the putative Zmg13 TATA box. No GUS RNA or enzyme expression was not detected in non-transformed tobacco. RNA and GUS histochemical analysis of the T1 generation confirmed that the temporal expression pattern of Zmg13-GUS transcription in tobacco followed that of the native gene in maize and that the Zmg13 promoter sequences from the maize gene are able correctly to direct genetically stable, tissue-specific gene expression in transgenic tobacco plants.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 229 (1991), S. 219-228 
    ISSN: 1617-4623
    Keywords: Glyceraldehyde-3-phosphate dehydrogenase ; Maize ; Development ; Isozymes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The distribution of the cytosolic glyceraldehyde-3-phosphate dehydrogenase gene family (Gpc) in the maize genome was investigated; a genetic variant of glyceraldehyde-3-phosphate dehydrogenase activity is also described. Restriction fragment length polymorphism analysis of an F2 population shows that the variant is not linked to the three known Gpc genes. However, this trait is linked to one of two genomic DNA fragments that hybridize to a fragment of the Gpc3 coding region, implying the existence of a fourth Gpc gene. Antibodies and cDNA clones were used to investigate the organ-specific expression of the Gpc genes. Results were compared with the expression of the alcohol dehydrogenase 1 (Adh1) gene. RNA and protein levels were examined in seedling roots and shoots, as well as the leaves, developing endosperm and embryo, and the aleurone. In general, it was found that Gpc3 expression behaves in parallel with Adh1 in these organs, and protein levels closely parallel that of RNA for each gene examined. Both Gpc3 and Adh1 show a marked increase in expression during endosperm development, reaching a maximum 15 days after pollination, but no expression is detected in the leaf. Gpc1 expression is similar to that of Gpc2, with an overall decrease in the level of RNA during endosperm development. This expression is discussed in terms of the common sequences found upstream of genes expressed in the developing maize seed.
    Type of Medium: Electronic Resource
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