Literature DB >> 26324435

Fluorescent In Situ Hybridization of Nuclear Bodies in Drosophila melanogaster Ovaries.

Zehra F Nizami1, Ji-Long Liu, Joseph G Gall.   

Abstract

Fluorescent in situ hybridization (FISH) is a technique for determining the cytological localization of RNA or DNA molecules. There are many approaches available for generating in situ hybridization probes and conducting the subsequent hybridization steps. Here, we describe a simple and reliable FISH method to label small RNAs (200-500 nucleotides in length) that are enriched in nuclear bodies in Drosophila melanogaster ovaries, such as Cajal bodies (CBs) and histone locus bodies (HLBs). This technique can also be applied to other Drosophila tissues, and to abundant mRNAs such as histone transcripts.

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Year:  2015        PMID: 26324435      PMCID: PMC5588913          DOI: 10.1007/978-1-4939-2851-4_10

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  12 in total

Review 1.  The Cajal body and histone locus body.

Authors:  Zehra Nizami; Svetlana Deryusheva; Joseph G Gall
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-05-26       Impact factor: 10.005

2.  Cajal bodies and histone locus bodies in Drosophila and Xenopus.

Authors:  Z F Nizami; S Deryusheva; J G Gall
Journal:  Cold Spring Harb Symp Quant Biol       Date:  2010-11-03

3.  Developmental and cell cycle regulation of the Drosophila histone locus body.

Authors:  Anne E White; Michelle E Leslie; Brian R Calvi; William F Marzluff; Robert J Duronio
Journal:  Mol Biol Cell       Date:  2007-04-18       Impact factor: 4.138

4.  U bodies are cytoplasmic structures that contain uridine-rich small nuclear ribonucleoproteins and associate with P bodies.

Authors:  Ji-Long Liu; Joseph G Gall
Journal:  Proc Natl Acad Sci U S A       Date:  2007-06-26       Impact factor: 11.205

5.  Reversible response of protein localization and microtubule organization to nutrient stress during Drosophila early oogenesis.

Authors:  Yuko Shimada; K Mahala Burn; Ryusuke Niwa; Lynn Cooley
Journal:  Dev Biol       Date:  2011-04-23       Impact factor: 3.582

6.  U bodies respond to nutrient stress in Drosophila.

Authors:  Mickey Buckingham; Ji-Long Liu
Journal:  Exp Cell Res       Date:  2011-09-12       Impact factor: 3.905

7.  U7 snRNA mutations in Drosophila block histone pre-mRNA processing and disrupt oogenesis.

Authors:  Ashley C Godfrey; Jeremy M Kupsco; Brandon D Burch; Ryan M Zimmerman; Zbigniew Dominski; William F Marzluff; Robert J Duronio
Journal:  RNA       Date:  2006-03       Impact factor: 4.942

8.  The Drosophila melanogaster Cajal body.

Authors:  Ji-Long Liu; Christine Murphy; Michael Buszczak; Sarah Clatterbuck; Robyn Goodman; Joseph G Gall
Journal:  J Cell Biol       Date:  2006-03-13       Impact factor: 10.539

9.  Novel small Cajal-body-specific RNAs identified in Drosophila: probing guide RNA function.

Authors:  Svetlana Deryusheva; Joseph G Gall
Journal:  RNA       Date:  2013-10-22       Impact factor: 4.942

10.  The endocycle controls nurse cell polytene chromosome structure during Drosophila oogenesis.

Authors:  K J Dej; A C Spradling
Journal:  Development       Date:  1999-01       Impact factor: 6.868

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  2 in total

1.  miR-275/305 cluster is essential for maintaining energy metabolic homeostasis by the insulin signaling pathway in Bactrocera dorsalis.

Authors:  Junfei Xie; Hao Chen; Wenping Zheng; Zhaohui Cai; Xiaoxue Li; Hongyu Zhang
Journal:  PLoS Genet       Date:  2022-10-05       Impact factor: 6.020

2.  Loss of the RNA trimethylguanosine cap is compatible with nuclear accumulation of spliceosomal snRNAs but not pre-mRNA splicing or snRNA processing during animal development.

Authors:  Lin Cheng; Yu Zhang; Yi Zhang; Tao Chen; Yong-Zhen Xu; Yikang S Rong
Journal:  PLoS Genet       Date:  2020-10-21       Impact factor: 5.917

  2 in total

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