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Regulation of X-linked gene expression during early mouse development by Rlim.

Feng Wang | JongDae Shin | Jeremy M Shea | Jun Yu | Ana Bošković | Meg Byron | Xiaochun Zhu | Alex K Shalek | Aviv Regev | Jeanne B Lawrence | Eduardo M Torres | Lihua J Zhu | Oliver J Rando | Ingolf Bach
eLife | 2016

Mammalian X-linked gene expression is highly regulated as female cells contain two and male one X chromosome (X). To adjust the X gene dosage between genders, female mouse preimplantation embryos undergo an imprinted form of X chromosome inactivation (iXCI) that requires both Rlim (also known as Rnf12) and the long non-coding RNA Xist. Moreover, it is thought that gene expression from the single active X is upregulated to correct for bi-allelic autosomal (A) gene expression. We have combined mouse genetics with RNA-seq on single mouse embryos to investigate functions of Rlim on the temporal regulation of iXCI and Xist. Our results reveal crucial roles of Rlim for the maintenance of high Xist RNA levels, Xist clouds and X-silencing in female embryos at blastocyst stages, while initial Xist expression appears Rlim-independent. We find further that X/A upregulation is initiated in early male and female preimplantation embryos.

Pubmed ID: 27642011

Associated grants

  • Agency: NICHD NIH HHS, United States
    Id: R01 HD080224
  • Agency: NCI NIH HHS, United States
    Id: R01 CA131158
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM053234
  • Agency: NIGMS NIH HHS, United States
    Id: R35 GM122597
  • Agency: NIDDK NIH HHS, United States
    Id: P30 DK032520
  • Agency: NIEHS NIH HHS, United States
    Id: DP1 ES025458

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This is a list of tools and resources that we have found mentioned in this publication.


Bioconductor (tool)

RRID:SCR_006442

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RRID:SCR_002105

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HTSeq (tool)

RRID:SCR_005514

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on February 28,2023. Software Python package that provides infrastructure to process data from high-throughput sequencing assays. While the main purpose of HTSeq is to allow you to write your own analysis scripts, customized to your needs, there are also a couple of stand-alone scripts for common tasks that can be used without any Python knowledge.

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edgeR (tool)

RRID:SCR_012802

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RRID:SCR_012828

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RRID:SCR_013035

Software tool for fast and high throughput alignment of shotgun cDNA sequencing reads generated by transcriptomics technologies. Fast splice junction mapper for RNA-Seq reads. Aligns RNA-Seq reads to mammalian-sized genomes using ultra high-throughput short read aligner Bowtie, and then analyzes mapping results to identify splice junctions between exons.TopHat2 is accurate alignment of transcriptomes in presence of insertions, deletions and gene fusions.

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RRID:MMRRC_029172-UNC

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