This is a post about Alternative Splicing. I've avoided using that term in the title because it's very misleading. Alternative splicing produces a number of different products (RNA or protein) from a single intron-containing gene. The phenomenon has been known for 35 years and there are quite a few very well-studied examples, including several where all of the splice regulatory factors have been characterized.
This seems like common sense to me but, unfortunately, most scientists disagree. They continue to refer to any example of splice variants as alternative splicing even though they might be just splicing errors. In fact, most of these scientists don't even consider the possibility of splicing errors. See the following posts for a more thorough discussion of this problem.
Debating alternative splicing (part I)
Debating alternative splicing (part II)
Debating alternative splicing (Part III)
Debating alternative splicing (Part IV)
His most recent paper employs the latest technology for detecting RNAs in a cell. The authors highlight the fact that they can detect very low abundance RNAs. They apply the technique to map all the RNAS complementary to the DNA on human chromosome 21. They choose three tissues; testis, brain, and kidney. Two of these tissues are well-known examples of noisy transcription.
The old RNA-Seq view is shown in the upper-right part of the image. A typical protein-coding gene produces a number of splice variants that I assume are examples of splicing errors. Mattick and his colleagues assume they are due to alternative splicing. The noncoding part of the genome is complementary to another set of transcipts with a limited set of splice variants. Mattick assumes these regions are genes and the RNAs are functional, although he has no proof of that. I assume that most of these RNA are spurious transcipts of junk DNA. This should be the default assumption.
The new view is derived from their more exhaustive analysis of very rare transcripts. There are more splice variants from protein-coding genes but the increase is not enormous. In contrast, there are many more variants RNAs from the rest of the genome and this includes an enormous diversity of different exons. The title of the paper say it all: Universal alternative splicing of noncoding exons. Here are the main conclusion of the paper ...
We propose that noncoding exons are functionally modular, with alternative splicing generating an enormous repetoire of potentially regulatory RNAs and a rich transcriptional reservoir for gene evolution. (abstract)Yes, it's true that one could envisage such a scenario. One can image many things, but the real question is not how potent your imagination is but whether it's realistic.
One can envision a scenario where individual noncoding exons interact independently with other biomolecules (proteins, RNAs and/or DNA-motifs), organizing these around the scaffold of a noncoding transcript. In this way, alternative isoforms could assemble different collections of binding partners to dynamically regulate cellular processes. (discussion)
Scenarios should be based on facts and not on wishful thinking. In this case there's a lot of evidence that most of our genome is junk. If you are going to propose that most of it contains genes for regulatory RNAs then you have an obligation to refute or discredit the evidence for junk. This paper doesn't do that.
Similarly, there are many good reasons to suspect that splice variants are mistakes in splicing. The variants are not conserved, most are present at less than one copy per cell, splicing errors are known to occur at relatively high frequency, and very few have been shown to have a function. The default assumption must be that they are junk RNA unless proven otherwise.
Mattick and his colleagues dismiss some of these objections using arguments that make no sense. The problem with this paper is that it is promoting an extraordinary claim without any serious evidence of function, let alone extraordinary evidence. I don't understand how it passed peer review. The data may be fine but the interpretation and the conclusions are not.
I think the tide is turning against Mattick and his supporters but perhaps that's just wishful thinking on my part. Take a look at the RNA variants in the lower right-hand corner of the figure. How many of you believe they represent exquisite fine-tuning of a regulatory RNA? How many of you think they are mostly transcriptional and splicing errors?
Deveson, I.W., Brunck, M.E., Blackburn, J., Tseng, E., Hon, T., Clark, T.A., Clark, M.B., Crawford, J., Dinger, M.E., Nielsen, L.K., Mattick, J.S., and Mercer, T.R. (2017) Universal alternative splicing of noncoding exons. Cell Systems, 6:(1-11). [doi: 10.1016/j.cels.2017.12.005]