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Artikel: Effects of spontaneous KitlSteel mutations on survival and red blood cells of mice.

Rajaraman, Sripriya / Wood, Lawrence K / Willhite, Dorian K / Russell, Liane B / Bedell, Mary A

Mammalian genome : official journal of the International Mammalian Genome Society

2003  Band 14, Heft 3, Seite(n) 168–174

Abstract: Kit ligand (Kitl), which is a member of the helical cytokine superfamily, is encoded by the Steel (Sl) locus of mice and is essential for the development of hematopoietic cells, germ cells, and melanocytes. A large series of Kitl(Sl) alleles has been ... ...

Abstract Kit ligand (Kitl), which is a member of the helical cytokine superfamily, is encoded by the Steel (Sl) locus of mice and is essential for the development of hematopoietic cells, germ cells, and melanocytes. A large series of Kitl(Sl) alleles has been described, including some that arose spontaneously and others that were induced by either chemical or radiation mutagenesis. Here we describe the nucleotide sequence alterations in two spontaneous Kitl(Sl) alleles. The Kitl(Sl-18R) allele has a point mutation that introduces a premature termination codon, and the encoded protein is expected to be null functionally. The Kitl(Sl-5R) allele has an in-frame deletion that results in deletion of amino acids at position 31 and 32 of Kitl. While both mutations exert severe effects on blood cells and survival of homozygous mice, these effects are slightly milder than those of a previously characterized spontaneous deletion allele, Kitl(Sl-gb). Examination of the survival of compound heterozygotes provided strong genetic evidence that the Kitl(Sl-18R) and Kitl(Sl-5R) mutants are null functionally for mouse survival.
Mesh-Begriff(e) Animals ; Erythrocytes/metabolism ; Mice ; Mutation ; Polymorphism, Genetic ; RNA, Messenger/metabolism ; Stem Cell Factor/genetics ; Stem Cell Factor/metabolism
Chemische Substanzen RNA, Messenger ; Stem Cell Factor
Sprache Englisch
Erscheinungsdatum 2003-03
Erscheinungsland United States
Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
ZDB-ID 1058547-3
ISSN 1432-1777 ; 0938-8990
ISSN (online) 1432-1777
ISSN 0938-8990
DOI 10.1007/s00335-002-2193-4
Signatur
Zs.A 3489: Hefte anzeigen Standort:
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