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  • AFLP  (2)
  • DNA-binding proteins  (1)
  • 1
    ISSN: 1573-8590
    Keywords: AFLP ; Artemia ; species
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geography
    Notes: Abstract Amplified Fragment Length Polymorphism (AFLP) markers were successfully employed to analyze 15Artemia species and strains for genetic diversity. AFLP markers are extremely sensitive to even a small sequence variation. They are stable and more polymorphic than RAPD. Twelve pairs of primer combinations were used to detect AFLP bands, of which 384 were polymorphic, and DNA fingerprintings were obtained by using silver staining. The polymorphism analysis leads us to the following conclusions: 1.Artemia tibetiana seems to differentiate fromA. sinica. 2. The parthenogenetic populations from inland salt lakes could follow an evolutionary path that is different from that of the coastal parthenogenetic populations.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-8590
    Keywords: AFLP ; Artemia ; species
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geography
    Notes: Abstract Amplified Fragment Length Polymorphism(AFLP) markers were successfully employed to analyze15 Artemia species and strains for geneticdiversity. AFLP markers are extremely sensitive toeven a small sequence variation. They are stable andmore polymorphic than RAPD. Twelve pairs of primercombinations were used to detect AFLP bands, of which384 were polymorphic, and DNA fingerprintings wereobtained by using silver staining. The polymorphismanalysis leads us to the following conclusions: 1. Artemia tibetiana seems to differentiate from A.sinica. 2. The parthenogenetic populations frominland salt lakes could follow an evolutionary paththat is different from that of the coastalparthenogenetic populations.
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  • 3
    ISSN: 1573-5028
    Keywords: cucumber ; cytokinin-responsive ; DNA-binding proteins ; hydroxypyruvate reductase ; transcription
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Transcription of the cucumber hpr-A gene is responsive to cytokinin and light. To investigate the molecular basis for transcriptional regulation by cytokinin, we have identified DNA sequences and proteins that may be involved in the regulation of hpr-A gene expression. Transient expression assays in etiolated cucumber cotyledons indicate that the 315 bp fragment (−382 to −67) contains sequences necessary for cytokinin responsiveness of the luciferase reporter gene. Band shift assays detected cytokinin-enhanced and -reduced protein binding sites in a 97 bp fragment (−382 to −285) upstream of the hpr-A gene. DNase I footprinting identified two protein-protected sites, a 15 bp sequence, 5′-AAATGACGAAAATGC-3′, that contains an as-1 TGACG motif found in other plant promoters, and a 13 bp sequence, 5′-AAGATTGATTGAG-3′, of unknown function. Two-dimensional band shift analysis of the cytokinin-responsive DNA protein complex revealed the presence of six DNA protein interactions. Band shift assays showed that cytokinin and light have different effects on the interaction of nuclear proteins to the 97 bp fragment of the hpr-A gene. These data suggest that cytokinin and light do not share identical signal transduction pathways in regulating hpr-A gene expression.
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