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
Filter
  • Electronic Resource  (2)
  • 1995-1999  (2)
  • 1955-1959
  • 1999  (1)
  • 1995  (1)
  • Normoxia  (1)
  • Plasmodium development  (1)
Material
  • Electronic Resource  (2)
Years
  • 1995-1999  (2)
  • 1955-1959
Year
  • 1999  (1)
  • 1995  (1)
  • 1
    ISSN: 1432-072X
    Keywords: Key words Slime moulds ; Physarum polycephalum ; Plasmodium development ; Differential gene expression ; Myosin ; Calcium-binding protein
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract During the life cycle of Physarum polycephalum, uninucleate amoebae develop into multinucleate syncytial plasmodia. These two cell types differ greatly in cellular organisation, behaviour and gene expression. Classical genetic analysis has identified the mating-type gene, matA, as the key gene controlling the initiation of plasmodium development, but nothing is known about the molecular events controlled by matA. In order to identify genes involved in regulating plasmodium formation, we constructed a subtracted cDNA library from cells undergoing development. Three genes that have their highest levels of expression during plasmodium development were identified: redA, redB (regulated in development) and mynD (myosin). Both redA and redB are single-copy genes and are not members of gene families. Although redA has no significant sequence similarities to known genes, redB has sequence similarity to invertebrate sarcoplasmic calcium-binding proteins. The mynD gene is closely related to type II myosin heavy-chain genes from many organisms and is one of a family of type II myosin genes in P. polycephalum. Our results indicate that many more red genes remain to be identified, some of which may play key roles in controlling plasmodium formation.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 164 (1995), S. 622-628 
    ISSN: 1432-136X
    Keywords: Protein turnover ; Normoxia ; Anoxia ; Perfused heart ; Turtle, Trachemys sp
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Protein turnover was studied under conditions of normoxia and anoxia in isolated perfused turtle (Trachemys (=Pseudemys) scripta elegans) hearts at 15 °C. Protein synthesis was measured by 3H-labelled phenylalanine incorporation into the protein pool. Protein degradation was studied using the protein synthesis inhibitor cycloheximide and measuring phenylalanine release from the heart. Heart rate, cardiac output and ventricle pressure development were unaffected by 2 h of anoxia. Protein synthesis rate was tenfold lower in turtle heart than in rat heart at their respective body temperatures. However, 1 h of anoxia did not affect the rate of protein synthesis in turle heat. RNA content of both ventricle and atria decreased after anoxic perfusion. Protein synthesis rates in atria were higher than those of ventricle under conditions of either anoxia or normoxia. Protein degradation rate did not change in cycloheximide-treated turtle hearts after 2 h of anoxia. These findings indicate that lack of oxygen per se does not affect protein turnover in the isolated perfused turtle heart. This feature presumably allows protein turnover to proceed in vivo during routine dives at elevated temperatures. Also, the turtle heart is a good model system to study the effects of anoxia on protein turnover without the potentially confounding factor of contractile failure. These hearts are very resistant to anoxia and well able to maintain contractility for extended periods of time.
    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...