Comment on " Is Dispensable for Mouse Development"


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Published in the journal: . PLoS Genet 12(12): e32767. doi:10.1371/journal.pgen.1006406
Category: Formal Comment
doi: 10.1371/journal.pgen.1006406

Summary

article has not abstract

Amandio et al. [1] reanalyzed a Hotair knockout (KO) mouse allele previously reported by Li et al. [2]. The authors evaluated the phenotypes in different genetic backgrounds, performed transcriptome profiling of cells derived from different tissues and developmental stages, and, based on such investigations, highlighted different potential regulatory mechanisms. (e.g., cis versus trans effects).

Li et al. analyzed Hotair KO on the C57BL/6 background and examined the lumbar and wrist skeletons. These phenotypes were examined because prior work ([3], also by Duboule lab) showed that a HoxD locus transgene caused lumbosacral homeotic transformation (lumbar 6 transformed to sacral 1, L6→S1, also termed L5 based on the last lumbar segment). In C57BL/6 background, Li et al. found 6% of wild-type (WT) animals had L5, whereas 58% of the Hotair KO mice have L5, consistent with an L6→S1 transformation [2]. Amandio et al. analyzed the Hotair KO in a mixed CBAxBL6 background. In this background, approximately 80% of WT animals already had L5, and there was no additional lumbar skeletal phenotype (e.g., L4) in the KO, which may not be surprising, as the Hotair expression domain is located more posteriorly. Amandio et al. also found lower frequency of a caudal skeletal transformation (C4) than reported by Li et al. and independently by Lai et al. in two Hotair-LacZ KO alleles [2,4]. Amandio et al. did not observe malformation of wrist bones reported by Li et al., although Li et al. performed histologic sections at multiple stages that may be more sensitive than whole mounts at one time point done in [1]. Genetic background has a profound influence on KO phenotypes [5], and this lesson extends to long noncoding RNAs (lncRNAs) [6].

Li et al. analyzed RNA expression and histone modification patterns from tail tip fibroblasts (TTF) obtained from newborn mice [2]. TTF were chosen because (i) they represented a relatively homogenous cell type with defined positional identity, (ii) single cell analysis showed most TTF cells expressed Hotair, and (iii) TTF allowed comparison with human fibroblasts in which human HOTAIR was characterized. Li et al. found derepression of HoxD and several imprinted genes in the KO. In contrast, Amandio et al. performed RNA-seq on dissected E12.5 embryo fragments and whole mount in situ hybridization on E12.5 embryos and did not detect changes in HoxD expression [1]. Each embryo fragment is expected to contain a variety of different cell types. Indeed, Amandio et al. identify hundreds of genes with apparent differences in expression between WT and KO in the CBAxBL6 background, and the largest gene derepression was observed in posterior trunk and genital tubercle, where Hotair expression is the highest in WT tissues. However, many gene expression differences were identified between WT and KO even in tissues that do not express Hotair; thus, it is unclear if such differences reflect direct effects of Hotair or technical variations from microdissection. Nonetheless, this information expands the potential genes affected in vivo, directly or indirectly, by Hotair deletion.

Hotair is located in the HoxC locus between Hoxc11 and Hoxc12. Amandio et al. focused on the HoxC locus, observed alterations in Hoxc11 expression domain, and discovered new transcribed regions at the junction of the Hotair deletion [1]. These cis effects should be taken into consideration in future studies and highlight the interweaved nature of regulatory elements and pervasive transcription in the Hox loci and in mammalian genomes. Future studies using ectopic Hotair transgene may be able to separate cis versus trans effects of the lncRNA. Additionally, focal promoter deletion or insertion of polyadenylation sequence to truncate lncRNA in a strand-specific manner may better target lncRNA transcription while minimally affecting its genomic locus in cis [7,8].


Zdroje

1. Amandio AR, Necsulea A, Joye E, Mascrez B, Duboule D. Hotair is dispensable for mouse development. PLoS Genet. 2016;this issue.

2. Li L, Liu B, Wapinski OL, Tsai MC, Qu K, Zhang J, et al. Targeted disruption of Hotair leads to homeotic transformation and gene derepression. Cell Rep. 2013;5(1):3–12. Epub 2013/10/01. PubMed Central PMCID: PMC4038295. doi: 10.1016/j.celrep.2013.09.003 24075995

3. Spitz F, Gonzalez F, Peichel C, Vogt TF, Duboule D, Zakany J. Large scale transgenic and cluster deletion analysis of the HoxD complex separate an ancestral regulatory module from evolutionary innovations. Genes Dev. 2001;15(17):2209–14. Epub 2001/09/07. PubMed Central PMCID: PMC312772. doi: 10.1101/gad.205701 11544178

4. Lai KM, Gong G, Atanasio A, Rojas J, Quispe J, Posca J, et al. Diverse Phenotypes and Specific Transcription Patterns in Twenty Mouse Lines with Ablated LincRNAs. PLoS ONE. 2015;10(4):e0125522. Epub 2015/04/25. PubMed Central PMCID: PMC4409293. doi: 10.1371/journal.pone.0125522 25909911

5. Threadgill DW, Dlugosz AA, Hansen LA, Tennenbaum T, Lichti U, Yee D, et al. Targeted disruption of mouse EGF receptor: effect of genetic background on mutant phenotype. Science. 1995;269(5221):230–4. Epub 1995/07/14. 7618084

6. Gomez JA, Wapinski OL, Yang YW, Bureau JF, Gopinath S, Monack DM, et al. The NeST Long ncRNA Controls Microbial Susceptibility and Epigenetic Activation of the Interferon-gamma Locus. Cell. 2013;152(4):743–54. Epub 2013/02/19. doi: 10.1016/j.cell.2013.01.015 23415224

7. Yin Y, Yan P, Lu J, Song G, Zhu Y, Li Z, et al. Opposing Roles for the lncRNA Haunt and Its Genomic Locus in Regulating HOXA Gene Activation during Embryonic Stem Cell Differentiation. Cell Stem Cell. 2015;16(5):504–16. Epub 2015/04/22. doi: 10.1016/j.stem.2015.03.007 25891907

8. Gutschner T, Baas M, Diederichs S. Noncoding RNA gene silencing through genomic integration of RNA destabilizing elements using zinc finger nucleases. Genome Res. 2011;21(11):1944–54. Epub 2011/08/17. PubMed Central PMCID: PMC3205578. doi: 10.1101/gr.122358.111 21844124

Štítky
Genetika Reprodukční medicína

Článek vyšel v časopise

PLOS Genetics


2016 Číslo 12

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