Miranda as a multidomain adapter linking apically localized inscuteable and basally localized Staufen and Prospero during asymmetric cell division in Drosophila
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作者:
Shen, CP
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机构:Univ Calif San Francisco, Dept Physiol, Howard Hughes Med Inst, San Francisco, CA 94143 USA
Shen, CP
Knoblich, JA
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机构:Univ Calif San Francisco, Dept Physiol, Howard Hughes Med Inst, San Francisco, CA 94143 USA
Knoblich, JA
Chan, YM
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机构:Univ Calif San Francisco, Dept Physiol, Howard Hughes Med Inst, San Francisco, CA 94143 USA
Chan, YM
Jiang, MM
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机构:Univ Calif San Francisco, Dept Physiol, Howard Hughes Med Inst, San Francisco, CA 94143 USA
Jiang, MM
Jan, LY
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机构:Univ Calif San Francisco, Dept Physiol, Howard Hughes Med Inst, San Francisco, CA 94143 USA
Jan, LY
Jan, YN
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机构:Univ Calif San Francisco, Dept Physiol, Howard Hughes Med Inst, San Francisco, CA 94143 USA
Jan, YN
机构:
[1] Univ Calif San Francisco, Dept Physiol, Howard Hughes Med Inst, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Biochem, Howard Hughes Med Inst, San Francisco, CA 94143 USA
Neuroblasts in the developing Drosophila CNS asymmetrically localize the cell fate determinants Numb and Prospero as well as prospero RNA to the basal cortex during mitosis. The localization of Prospero requires the function of inscuteable and miranda, whereas prospero RNA localization requires inscuteable and staufen function. We demonstrate that Miranda contains multiple functional domains: an amino-terminal asymmetric localization domain, which interacts with Inscuteable, a central Numb interaction domain, and a more carboxy-terminal Prospero interaction domain. We also show that Miranda and Staufen have similar subcellular localization patterns and interact in vitro. Furthermore, miranda function is required for the asymmetric localization of Staufen. Miranda localization is disrupted by the microfilament disrupting agent latrunculin A. Our results suggest that Miranda directs the basal cortical localization of multiple molecules, including Staufen and prospero RNA, in mitotic neuroblasts in an actin-dependent manner.
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UNIV CALIF SAN FRANCISCO, DEPT PHYSIOL & BIOCHEM, SAN FRANCISCO, CA 94143 USAUNIV CALIF SAN FRANCISCO, DEPT PHYSIOL & BIOCHEM, SAN FRANCISCO, CA 94143 USA
UEMURA, T
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SHEPHERD, S
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UNIV CALIF SAN FRANCISCO, DEPT PHYSIOL & BIOCHEM, SAN FRANCISCO, CA 94143 USAUNIV CALIF SAN FRANCISCO, DEPT PHYSIOL & BIOCHEM, SAN FRANCISCO, CA 94143 USA
SHEPHERD, S
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ACKERMAN, L
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UNIV CALIF SAN FRANCISCO, DEPT PHYSIOL & BIOCHEM, SAN FRANCISCO, CA 94143 USAUNIV CALIF SAN FRANCISCO, DEPT PHYSIOL & BIOCHEM, SAN FRANCISCO, CA 94143 USA
ACKERMAN, L
;
JAN, LY
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UNIV CALIF SAN FRANCISCO, DEPT PHYSIOL & BIOCHEM, SAN FRANCISCO, CA 94143 USAUNIV CALIF SAN FRANCISCO, DEPT PHYSIOL & BIOCHEM, SAN FRANCISCO, CA 94143 USA
JAN, LY
;
JAN, YN
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机构:
UNIV CALIF SAN FRANCISCO, DEPT PHYSIOL & BIOCHEM, SAN FRANCISCO, CA 94143 USAUNIV CALIF SAN FRANCISCO, DEPT PHYSIOL & BIOCHEM, SAN FRANCISCO, CA 94143 USA
机构:
UNIV CALIF SAN FRANCISCO, DEPT PHYSIOL & BIOCHEM, SAN FRANCISCO, CA 94143 USAUNIV CALIF SAN FRANCISCO, DEPT PHYSIOL & BIOCHEM, SAN FRANCISCO, CA 94143 USA
UEMURA, T
;
SHEPHERD, S
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机构:
UNIV CALIF SAN FRANCISCO, DEPT PHYSIOL & BIOCHEM, SAN FRANCISCO, CA 94143 USAUNIV CALIF SAN FRANCISCO, DEPT PHYSIOL & BIOCHEM, SAN FRANCISCO, CA 94143 USA
SHEPHERD, S
;
ACKERMAN, L
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机构:
UNIV CALIF SAN FRANCISCO, DEPT PHYSIOL & BIOCHEM, SAN FRANCISCO, CA 94143 USAUNIV CALIF SAN FRANCISCO, DEPT PHYSIOL & BIOCHEM, SAN FRANCISCO, CA 94143 USA
ACKERMAN, L
;
JAN, LY
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UNIV CALIF SAN FRANCISCO, DEPT PHYSIOL & BIOCHEM, SAN FRANCISCO, CA 94143 USAUNIV CALIF SAN FRANCISCO, DEPT PHYSIOL & BIOCHEM, SAN FRANCISCO, CA 94143 USA
JAN, LY
;
JAN, YN
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UNIV CALIF SAN FRANCISCO, DEPT PHYSIOL & BIOCHEM, SAN FRANCISCO, CA 94143 USAUNIV CALIF SAN FRANCISCO, DEPT PHYSIOL & BIOCHEM, SAN FRANCISCO, CA 94143 USA