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Comprehensive analysis of mammalian miRNA* species and their role in myeloid cells.

Kuchenbauer, Florian (author)
Mah, Sarah M (author)
Heuser, Michael (author)
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McPherson, Andrew (author)
Rüschmann, Jens (author)
Rouhi, Arefeh (author)
Berg, Tobias (author)
Bullinger, Lars (author)
Argiropoulos, Bob (author)
Morin, Ryan D (author)
Lai, David (author)
Starczynowski, Daniel T (author)
Karsan, Aly (author)
Eaves, Connie J (author)
Watahiki, Akira (author)
Wang, Yuzhuo (author)
Aparicio, Samuel A (author)
Ganser, Arnold (author)
Krauter, Jürgen (author)
Döhner, Hartmut (author)
Döhner, Konstanze (author)
Marra, Marco A (author)
Camargo, Fernando D (author)
Palmqvist, Lars, 1965 (author)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för klinisk kemi och transfusionsmedicin,Institute of Biomedicine, Department of Clinical Chemistry and Transfusion Medicine
Buske, Christian (author)
Humphries, R Keith (author)
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 (creator_code:org_t)
American Society of Hematology, 2011
2011
English.
In: Blood. - : American Society of Hematology. - 1528-0020 .- 0006-4971. ; 118:12, s. 3350-8
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Processing of pre-miRNA through Dicer1 generates an miRNA duplex that consists of an miRNA and miRNA* strand. Despite the general view that miRNA*s have no functional role, we further investigated miRNA* species in 10 deep-sequencing libraries from mouse and human tissue. Comparisons of miRNA/miRNA* ratios across the miRNA sequence libraries revealed that 50% of the investigated miRNA duplexes exhibited a highly dominant strand. Conversely, 10% of miRNA duplexes showed a comparable expression of both strands, whereas the remaining 40% exhibited variable ratios across the examined libraries, as exemplified by miR-223/miR-223* in murine and human cell lines. Functional analyses revealed a regulatory role for miR-223* in myeloid progenitor cells, which implies an active role for both arms of the miR-223 duplex. This was further underscored by the demonstration that miR-223 and miR-223* targeted the insulin-like growth factor 1 receptor/phosphatidylinositol 3-kinase axis and that high miR-223* levels were associated with increased overall survival in patients with acute myeloid leukemia. Thus, we found a supporting role for miR-223* in differentiating myeloid cells in normal and leukemic cell states. The fact that the miR-223 duplex acts through both arms extends the complexity of miRNA-directed gene regulation of this myeloid key miRNA.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Hematologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Hematology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Medical Genetics (hsv//eng)

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