scholarly journals Stable intronic sequence RNAs (sisRNAs) are selected regions in introns with distinct properties

BMC Genomics ◽  
2020 ◽  
Vol 21 (1) ◽  
Author(s):  
Jing Jin ◽  
Ximiao He ◽  
Elena Silva
Keyword(s):  
2009 ◽  
Vol 52 (3) ◽  
pp. 191 ◽  
Author(s):  
Paola Zago ◽  
Marco Baralle ◽  
Youhna M. Ayala ◽  
Natasa Skoko ◽  
Serena Zacchigna ◽  
...  

2018 ◽  
Vol 115 (34) ◽  
pp. E7970-E7977 ◽  
Author(s):  
Gaëlle J. S. Talhouarne ◽  
Joseph G. Gall

Most intronic RNAs are degraded within seconds or minutes after their excision from newly formed transcripts. However, stable intronic sequence RNAs (sisRNAs) have been described from oocytes of the frog Xenopus, from Drosophila embryos, and from human cell lines. In Xenopus oocytes, sisRNAs are abundant in both the nucleus and cytoplasm, they occur in the form of lariats, and they are stable for days. In this study we demonstrate that cytoplasmic sisRNAs are also found in human, mouse, chicken, and zebrafish cells. They exist as circular (lariat) molecules, mostly 100–500 nucleotides in length, and are derived from many housekeeping genes. They tend to have an unusual cytosine branchpoint (with the exception of those from the frog). Stable lariats are exported from the nucleus to the cytoplasm by the NXF1/NXT1 system, demonstrating that their presence in the cytoplasm is not due to passive diffusion. Lariats in the cytoplasm are not associated with transcripts of the genes from which they are derived. The biological significance of cytoplasmic sisRNAs remains obscure.


2015 ◽  
Vol 212 (12) ◽  
pp. 21212OIA99
Author(s):  
Jun Wei Pek ◽  
Ismail Osman ◽  
Mandy Li-Ian Tay ◽  
Ruther Teo Zheng

2000 ◽  
Vol 110 (4) ◽  
pp. 867-870 ◽  
Author(s):  
Masako Hirota ◽  
Eiko Hidaka ◽  
Ichiro Ueno ◽  
Masayo Ishikawa ◽  
Naoko Asano ◽  
...  

Genome ◽  
2012 ◽  
Vol 55 (1) ◽  
pp. 75-79 ◽  
Author(s):  
Hiroyo Kagami ◽  
Hironori Nagano ◽  
Yoshiya Takahashi ◽  
Tetsuo Mikami ◽  
Tomohiko Kubo

Introns may be considered as optional because they are removed from mRNA molecules, but introns are fairly preserved for unknown reasons. Previously, the mitochondrial rps3 gene of sugar beet ( Beta vulgaris L., Caryophyllales) was shown to represent a unique example of an intron loss. We have determined the distribution of the rps3 intron in 19 Caryophyllalean species. The intron was absent from the Amaranthaceae and the Achatocarpaceae. In the Caryophyllaceae, Dianthus japonicus rps3 was pseudogenized, but the intronic sequence was retained. Intact intron-bearing rps3 copies were cloned from Portulaca grandiflora and Myrtillocactus geometrizans , members of the sister clade of the Amaranthaceae–Achatocarpaceae–Caryophyllaceae clade. Most of the C-to-U RNA-editing sites in P. grandiflora and M. geometrizans rps3 transcripts were homologous in the two species, as well as in the sugar beet rps3, which, unlike the other 12 rps3 transcripts, lacks editing in the exonic regions around the intron. Provided that the loss of editing preceded the loss of rps3 intron, it appears conceivable that a requirement for editing could have prevented the loss of group II introns retained in angiosperm mitochondrial genomes. This interpretation is an alternative to the conventional one that views the loss of editing as a mere trace of RNA-mediated gene conversion.


2006 ◽  
Vol 133 (3) ◽  
pp. 270-275 ◽  
Author(s):  
Ioannis Panagopoulos ◽  
Bodil Strombeck ◽  
Margareth Isaksson ◽  
Jesper Heldrup ◽  
Tor Olofsson ◽  
...  

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