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Telomere length varies substantially between blood cell types in a reptile

Artikel i vetenskaplig tidskrift
Författare Mats Olsson
N. J. Geraghty
E. Wapstra
M. Wilson
Publicerad i Royal Society Open Science
Volym 7
Nummer/häfte 6
Sidor 9
ISSN 2054-5703
Publiceringsår 2020
Publicerad vid Institutionen för biologi och miljövetenskap
Sidor 9
Språk en
Länkar dx.doi.org/10.1098/rsos.192136
Ämnesord telomeres, blood cell type, nucleated versus non-nucleated, lizard, Ctenophorus pictus, dynamics, stress, senescence, lizard, costs, link, Science & Technology - Other Topics
Ämneskategorier Biologiska vetenskaper

Sammanfattning

Telomeres are repeat sequences of non-coding DNA-protein molecules that cap or intersperse metazoan chromosomes. Interest in telomeres has increased exponentially in recent years, to now include their ongoing dynamics and evolution within natural populations where individuals vary in telomere attributes. Phylogenetic analyses show profound differences in telomere length across non-model taxa. However, telomeres may also differ in length within individuals and between tissues. The latter becomes a potential source of error when researchers use different tissues for extracting DNA for telomere analysis and scientific inference. A commonly used tissue type for assessing telomere length is blood, a tissue that itself varies in terms of nuclear content among taxa, in particular to what degree their thrombocytes and red blood cells (RBCs) contain nuclei or not. Specifically, when RBCs lack nuclei, leucocytes become the main source of telomeric DNA. RBCs and leucocytes differ in lifespan and how long they have been exposed to 'senescence' and erosion effects. We report on a study in which cells in whole blood from individual Australian painted dragon lizards (Ctenophorus pictus) were identified using flow cytometry and their telomere length simultaneously measured. Lymphocyte telomeres were on average 270% longer than RBC telomeres, and in azurophils (a reptilian monocyte), telomeres were more than 388% longer than those in RBCs. If this variation in telomere length among different blood cell types is a widespread phenomenon, and DNA for comparative telomere analyses are sourced from whole blood, evolutionary inference of telomere traits among taxa may be seriously complicated by the blood cell type comprising the main source of DNA.

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