Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 41 (1985), S. 1311-1319 
    ISSN: 1420-9071
    Keywords: Germ line—soma differentiation ; chromatin diminution ; gene loss ; satellite DNA ; molecular embryology ; nematology
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The early ontogenetic segregation of germ line and somatic cells in the animal kingdom is phylogenetically very old and represents probably the first step in differentiation. While this phenomenon has been shown to occur in various animal phyla, it seems to be completely msssing in the plant kingdom. In several animal species, the segregation of the germ and somatic cell lines is accompanied by the loss of whole or parts of chromosomes in the presumptive somatic cells. The cause of the chromatin diminution process as well as the significance of the germ line limited DNA sequences in species undergoing chromatin or chromosome loss still remain unknown. However, using modern biochemical and molecular biological techniques, it has become possible to analyze the process of chromatin diminution and the composition of the germ line specific DNA sequences at the molecular level. InAscaris lumbricoides, about a quarter of the total amount of germ line DNA is eliminated from the presumptive somatic cells during chromatin diminution. Hybridization experiments revealed that germ line and somatic DNA contain the same percentage of 18S+28S rRNA genes. Therefore, chromatin diminution does not serve to discard large amounts of rRNA-coding genes from the germ line cells. On the other hand, over 99%, but not all satellite DNA sequences present in the germ line genome, are expelled from the presumptive somatic cells by chromatin diminution. Molecular cloning and sequence analysis of different restriction endonuclease fragments isolated from the germ line satellite DNA indicated that this eliminated satellite is composed of a whole set of related variant sequences, which differ by small deletions, insertions and single base substitutions. Members of the same variant class are tandemly linked and therefore physically separated from other variant classes. By comparing all the determined sequences, it was possible to establish a 121 bp long and AT rich consensus sequence which itself exhibits an 11 bp long internal short range periodicity. We have no indication for transcriptional activity of the satellite DNA sequences at any stage or tissue tested. Evidence is accumulating that the eliminated DNA contains also other DNA sequences apart from the class of highly repetitive satellite DNA.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1432-2048
    Keywords: Gene expression ; Nitrate ; Nitrite-reductase ; Phytochrome ; Transgenic tobacco ; Nicotiana
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Deletion analysis of the nitrite-reductase (NiR) promoter from spinach (Spinacia oleracea L.) fused to theβ-glucuronidase (GUS) reporter gene and introduced into tobacco (Nicotiana tabacum L., cv. Coker 176) indicates that basic elements required for light- and nitrate-dependent expression of the reporter are located within the promoter sequence -200/+131 relative to the transcription-initiation site. Detailed analysis indicates that positive regulatory elements exist between -200 and-330 as well as between -1450 and -1730, stimulating the level of GUS gene expression under all experimental conditions. Induction/reversion light-pulse experiments show that the promoter sequence -200/+131 suffices for phytochrome-mediated expression of the reporter gene. The observation that the NiR promoter from spinach exhibits full reversibility in transgenic tobacco confirms the previous conclusion that the NiR promoter from spinach fused to a GUS reporter gene and introduced into tobacco responds to nitrate and phytochrome as would be expected for tobacco (host) and not as would be expected for spinach (donor). When the plastids were damaged by photooxidation in the presence of Norflurazon, GUS activity levels were reduced to the same extent for all NiR-promoter/GUS fusions tested, indicating that the promoter region involved in the action of the ‘plastidic factor’ is between -200 and +131. The GUS gene expression under the control of the CaMV-35S promoter is not affected by light, nitrate or the ‘plastidic factor’.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    ISSN: 1432-2048
    Keywords: Gene expression ; Nitrate ; Nitrite-reductase ; Phytochrome ; Transgenic tobacco ; Nicotiana
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Deletion analysis of the nitrite-reductase (NiR) promoter from spinach (Spinacia oleracea L.) fused to the β-glucuronidase (GUS) reporter gene and introduced into tobacco (Nicotiana tabacum L., cv. Coker 176) indicates that basic elements required for light- and nitrate-dependent expression of the reporter are located within the promoter sequence -200/+131 relative to the transcription-initiation site. Detailed analysis indicates that positive regulatory elements exist between -200 and-330 as well as between -1450 and -1730, stimulating the level of GUS gene expression under all experimental conditions. Induction/reversion light-pulse experiments show that the promoter sequence -200/+131 suffices for phytochrome-mediated expression of the reporter gene. The observation that the NiR promoter from spinach exhibits full reversibility in transgenic tobacco confirms the previous conclusion that the NiR promoter from spinach fused to a GUS reporter gene and introduced into tobacco responds to nitrate and phytochrome as would be expected for tobacco (host) and not as would be expected for spinach (donor). When the plastids were damaged by photooxidation in the presence of Norflurazon, GUS activity levels were reduced to the same extent for all NiR-promoter/GUS fusions tested, indicating that the promoter region involved in the action of the ‘plastidic factor’ is between -200 and +131. The GUS gene expression under the control of the CaMV-35S promoter is not affected by light, nitrate or the ‘plastidic factor’.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...