Literature DB >> 16143607

The HhH2/NDD domain of the Drosophila Nod chromokinesin-like protein is required for binding to chromosomes in the oocyte nucleus.

Wei Cui1, R Scott Hawley.   

Abstract

Nod is a chromokinesin-like protein that plays a critical role in segregating achiasmate chromosomes during female meiosis. The C-terminal half of the Nod protein contains two putative DNA-binding domains. The first of these domains, known as the HMGN domain, consists of three tandemly repeated high-mobility group N motifs. This domain was previously shown to be both necessary and sufficient for binding of the C-terminal half of Nod to mitotic chromosomes in embryos. The second putative DNA-binding domain, denoted HhH(2)/NDD, is a helix-hairpin-helix(2)/Nod-like DNA-binding domain. Although the HhH(2)/NDD domain is not required or sufficient for chromosome binding in embryos, several well-characterized nod mutations have been mapped in this domain. To characterize the role of the HhH(2)/NDD domain in mediating Nod function, we created a series of UAS-driven transgene constructs capable of expressing either a wild-type Nod-GFP fusion protein or proteins in which the HhH(2)/NDD domain had been altered by site-directed mutagenesis. Although wild-type Nod-GFP localizes to the oocyte chromosomes and rescues the segregation defect in nod mutant oocytes, two of three proteins carrying mutants in the HhH(2)/NDD domain fail to either rescue the nod mutant phenotype or bind to oocyte chromosomes. However, these mutant proteins do bind to the polytene chromosomes in nurse-cell nuclei and enter the oocyte nucleus. Thus, even though the HhH(2)/NDD domain is not essential for chromosome binding in other cell types, it is required for chromosome binding in the oocyte. These HhH(2)/NDD mutants also block the localization of Nod to the posterior pole of stage 9-10A oocytes, a process that is thought to facilitate the interaction of Nod with the plus ends of microtubules (Cui et al. 2005). This observation suggests that the Nod HhH2/NDD domain may play other roles in addition to binding Nod to meiotic chromosomes.

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Year:  2005        PMID: 16143607      PMCID: PMC1456107          DOI: 10.1534/genetics.105.047464

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  47 in total

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4.  Chromosome elasticity and mitotic polar ejection force measured in living Drosophila embryos by four-dimensional microscopy-based motion analysis.

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Journal:  Curr Biol       Date:  2001-04-17       Impact factor: 10.834

5.  The alpha subunit of E. coli RNA polymerase activates RNA binding by NusA.

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6.  The Xenopus chromokinesin Xkid is essential for metaphase chromosome alignment and must be degraded to allow anaphase chromosome movement.

Authors:  H Funabiki; A W Murray
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7.  The fusome organizes the microtubule network during oocyte differentiation in Drosophila.

Authors:  N C Grieder; M de Cuevas; A C Spradling
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8.  The chromokinesin Kid is necessary for chromosome arm orientation and oscillation, but not congression, on mitotic spindles.

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9.  Mutations in the alpha-tubulin 67C gene specifically impair achiasmate segregation in Drosophila melanogaster.

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10.  Reciprocal localization of Nod and kinesin fusion proteins indicates microtubule polarity in the Drosophila oocyte, epithelium, neuron and muscle.

Authors:  I E Clark; L Y Jan; Y N Jan
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  8 in total

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2.  Drosophila Nod protein binds preferentially to the plus ends of microtubules and promotes microtubule polymerization in vitro.

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3.  WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney Disease.

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Journal:  Hum Mutat       Date:  2015-08-06       Impact factor: 4.878

4.  An analysis of univalent segregation in meiotic mutants of Arabidopsis thaliana: a possible role for synaptonemal complex.

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Journal:  Genetics       Date:  2006-12-06       Impact factor: 4.562

5.  ATPase cycle of the nonmotile kinesin NOD allows microtubule end tracking and drives chromosome movement.

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Review 6.  The Ran Pathway in Drosophila melanogaster Mitosis.

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Journal:  Front Cell Dev Biol       Date:  2015-11-26

7.  NOD is a plus end-directed motor that binds EB1 via a new microtubule tip localization sequence.

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Journal:  J Cell Biol       Date:  2018-06-13       Impact factor: 10.539

Review 8.  The functions of kinesin and kinesin-related proteins in eukaryotes.

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  8 in total

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