SLC25A25-AS1

Species: Homo sapiens

Position: chr9: 128108580-128118734

Known as: SLC25A25-AS1 , ENSG00000234771

Transcript: NR_033374 , ENST00000418747

Sequence: Download

Description:

Loss-of-function (LOF) methods such as RNA interference (RNAi), antisense oligonucleotides or CRISPR-based genome editing provide unparalleled power for studying the biological function of genes. However, depletion of lncRNA with unknown function using different LOF methods can lead to different biological conclusions. SLC25A25-AS1 was choosed as a spliced and intragenic lncRNA with three promoters and a single 3' polyadenylation site. Among all ENCODE cell lines, SLC25A25-AS1 was most highly expressed in the nucleus of HeLa cells. The genomic locus was actively transcribed based on the presence of both histone H3 lysine 4 trimethylated (H3K4me3) and histone H3 lysine 27 acetylated (H3K27ac) histones at the predicted SLC25A25-AS1 locus. Both LNA oligonucleotides and CRISPRi guides achieved over 50% depletion. But, we observed a signifcant mitotic delay after LNA-mediated knockdown of SLC25A25-AS1, whereas no such effect was observed with the CRISPRi-based methods.



sgRNAs

sgRNA_ID Sequence Position (Chr) Position (Lnc) Length PAM Type Validity Cell line Note Ref.
sgRNA1 GATGGAGAATGTAAGGGTAC 128118725-128118744(+) gene body (near 5') 20 AGG CRISPRi Experimental validated Hela NA [1]
sgRNA2 TGCAGAGAACGGAGGCATGC 128118678-128118697(+) gene body (near 5') 20 AGG CRISPRi Experimental validated Hela NA [1]

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Links

lncRNA Function:

sgRNA Design Tool:

Reference

1. Stojic L, Lun ATL, Mangei J, Mascalchi P, Quarantotti V, et al. (2018). Specificity of RNAi, LNA and CRISPRi as loss-of-function methods in transcriptional analysis. Nucleic Acids Res.