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Titolo:
Mesodermal patterning defect in mice lacking the Ste20 NCK interacting kinase (NIK)
Autore:
Xue, YZ; Wang, XZ; Li, Z; Gotoh, N; Chapman, D; Skolnik, EY;
Indirizzi:
NYU, Med Ctr, Skirball Inst Biomol Med, Dept Pharmacol, New York, NY 10016USA NYU New York NY USA 10016 omol Med, Dept Pharmacol, New York, NY 10016USA Univ Pittsburgh, Dept Biol Sci, Pittsburgh, PA 15260 USA Univ Pittsburgh Pittsburgh PA USA 15260 iol Sci, Pittsburgh, PA 15260 USA
Titolo Testata:
DEVELOPMENT
fascicolo: 9, volume: 128, anno: 2001,
pagine: 1559 - 1572
SICI:
0950-1991(200105)128:9<1559:MPDIML>2.0.ZU;2-2
Fonte:
ISI
Lingua:
ENG
Soggetto:
N-TERMINAL KINASE; GERMINAL CENTER KINASE; FOCAL ADHESION KINASE; PHOTORECEPTOR AXON GUIDANCE; SIGNAL-TRANSDUCTION PATHWAY; GASTRULATING MOUSE EMBRYO; SH2/SH3 ADAPTER PROTEIN; CELL SHEET MOVEMENT; PARAXIAL MESODERM; EXPRESSION PATTERN;
Keywords:
Ste20 kinase; NCK interacting kinase (NIK); misshapen; gastrulation; knockout; N-terminal JUN kinase (JNK); mouse;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Life Sciences
Citazioni:
76
Recensione:
Indirizzi per estratti:
Indirizzo: Skolnik, EY NYU, Med Ctr, Skirball Inst Biomol Med, Dept Pharmacol, 540 1st Ave, New York, NY 10016 USA NYU 540 1st Ave New York NY USA 10016 , New York, NY 10016 USA
Citazione:
Y.Z. Xue et al., "Mesodermal patterning defect in mice lacking the Ste20 NCK interacting kinase (NIK)", DEVELOPMENT, 128(9), 2001, pp. 1559-1572

Abstract

We have previously shown that the Drosophila Ste20 kinase encoded by misshapen (msn) is an essential gene in Drosophila development. msn function is required to activate the Drosophila c-Jun N-terminal kinase (JNK), basket (Bsk), to promote dorsal closure of the Drosophila embryo. Later in development, msn expression is required in photoreceptors in order for their axons to project normally, A mammalian homolog of msn, the NCK-interacting kinase(NIK) (recently renamed to mitogen-activated protein kinase kinase kinase kinase 4; Map4k4), has been shown to activate JNK and to bind the SH3 domains of the SH2/SH3 adapter NCK, To determine whether NIK also plays an essential role in mammalian development, we created mice deficient in NIK by homologous recombination at the Nik gene. Nik(-/-) mice die postgastrulation between embryonic day (E) 9.5 and E10.5. The most striking phenotype in Nik(-/-) embryos is the failure of mesodermal and endodermal cells that arise from the anterior end of the primitive streak (PS) to migrate to their correct location. As a result Nik(-/-) embryos fail to develop somites or a hindgut and are truncated posteriorly, interestingly, chimeric analysis demonstrated that NIK has a cell nonautonomous function in stimulating migration of presomitic mesodermal cells away from the PS and a second cell autonomousfunction in stimulating the differentiation of presomitic mesoderm into dermomyotome. These findings indicate that despite the large number of Ste20 kinases in mammalian cells, members of this family play essential nonredundant function in regulating specific signaling pathways. In addition, these studies provide evidence that the signaling pathways regulated by these kinases are diverse and not limited to the activation of JNK because mesodermal and somite development are not perturbed in JNK1-, and JNK2-deficient mice.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 30/11/20 alle ore 11:39:08