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. 2012 Apr 23:3:60.
doi: 10.3389/fgene.2012.00060. eCollection 2012.

Dark Matter RNA: Existence, Function, and Controversy

Affiliations

Dark Matter RNA: Existence, Function, and Controversy

Philipp Kapranov et al. Front Genet. .

Abstract

The mysteries surrounding the ∼97-98% of the human genome that does not encode proteins have long captivated imagination of scientists. Does the protein-coding, 2-3% of the genome carry the 97-98% as a mere passenger and neutral "cargo" on the evolutionary path, or does the latter have biological function? On one side of the debate, many commentaries have referred to the non-coding portion of the genome as "selfish" or "junk" DNA (Orgel and Crick, 1980), while on the other side, authors have argued that it contains the real blueprint for organismal development (Penman, 1995; Mattick, 2003), and the mechanisms of developmental complexity. Thus, this question could be referred to without much exaggeration as the most important issue in genetics today.

Keywords: dark matter RNA; gene; genomics; intronic RNA; linc; non-coding; transcriptome; vlinc.

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Figures

Figure 1
Figure 1
Types of RNA molecules derived from annotated and unannotated loci that constitute “dark matter” RNAs.
Figure 2
Figure 2
Coverage of the genome by “dark matter” RNAs. (A) Information currently available about the regions of dark matter transcription and the actual RNA molecules made from these region comes from various types of experiments and databases. There is relatively little overlap between these different databases suggesting that the actual extend of dark matter transcription is far greater than any one database suggests. (B) A theoretical curve showing expected results of the fraction of the genome that is transcribed as a function of the number of biological sources whose RNA is profiled. The coverage of transcribed genome by protein coding genes including their introns is 42% and lincRNAs bring it up to 58%. However, the full extent of the transcribed genome is expected to be much greater than that.

References

    1. Affymetrix/CSHL ENCODE Project (2009). Post-transcriptional processing generates a diversity of 5’-modified long and short RNAs. Nature 457, 1028–1032 10.1038/nature07759 - DOI - PMC - PubMed
    1. Amaral P. P., Clark M. B., Gascoigne D. K., Dinger M. E., Mattick J. S. (2011). lncRNAdb: a reference database for long noncoding RNAs. Nucleic Acids Res. 39, D146–D151 10.1093/nar/gkr745 - DOI - PMC - PubMed
    1. Askarian-Amiri M. E., Crawford J., French J. D., Smart C. E., Smith M. A., Clark M. B., Ru K., Mercer T. R., Thompson E. R., Lakhani S. R., Vargas A. C., Campbell I. G., Brown M. A., Dinger M. E., Mattick J. S. (2011). SNORD-host RNA Zfas1 is a regulator of mammary development and a potential marker for breast cancer. RNA 17, 878–891 10.1261/rna.2528811 - DOI - PMC - PubMed
    1. Baillie J. K., Barnett M. W., Upton K. R., Gerhardt D. J., Richmond T. A., De Sapio F., Brennan P. M., Rizzu P., Smith S., Fell M., Talbot R. T., Gustincich S., Freeman T. C., Mattick J. S., Hume D. A., Heutink P., Carninci P., Jeddeloh J. A., Faulkner G. J. (2011). Somatic retrotransposition alters the genetic landscape of the human brain. Nature 479, 534–537 10.1038/nature10531 - DOI - PMC - PubMed
    1. Bertone P., Stolc V., Royce T. E., Rozowsky J. S., Urban A. E., Zhu X., Rinn J. L., Tongprasit W., Samanta M., Weissman S., Gerstein M., Snyder M. (2004). Global identification of human transcribed sequences with genome tiling arrays. Science 306, 2242–2246 10.1126/science.1103388 - DOI - PubMed

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