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T. Ryan GregoryRSS Feed of this column.

I am an evolutionary biologist specializing in genome size evolution at the University of Guelph in Guelph, Ontario, Canada. Be sure to visit Evolver Zone

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Blogroll

I have promised to move some "classic Genomicron" posts to this new page, but in the meantime here is a list of what I consider the most significant posts from the last year.

For readers who have been following the blog, this may highlight anything you missed, or maybe will be a chance to revisit some older favourites1. (And please update your blogroll to http://www.scientificblogging.com/genomicron)

For new readers, it provides a sense of what you can expect from this blog.

Either way, please enjoy.

 

Basic concepts:

This is interesting. You know, in a "I kinda wish I hadn't seen that" sort of way... Hat tip: Science After Sunclipse

Some exciting news!

After reflecting on the future of Genomicron, I have decided to move it to the Scientific Blogging network. Please update your links and keep reading!

Genomicron has recently moved to its new home here on the Scientific Blogging network from its original location. If you are a regular reader, I hope you will like the new look. If you're just finding the blog now, I hope you enjoy reading it! As always, my goal will be to post accessible and informative posts about evolution, genome biology, and the life sciences in general. Welcome to Genomicron 2.0.

 

Evolutionary trees, or "phylogenies", are a major part of modern evolutionary science. They depict hypotheses regarding the relationships among taxa, and are therefore important in reconstructions of the historical path of evolution (Gregory 2008a,b).

Various approaches can be taken to formulating phylogenetic hypotheses, including analyses based on morphological, fossil, and/or molecular data. These methods often agree well, but sometimes one or another can throw up some surprises and challenge previous hypotheses about the relationships among groups of organisms.

Reconstructing the tree of life is a difficult and complicated process, and one should expect there to be significant refinements and revisions along the way. This is especially true of the deepest branches of the tree, which are often the most difficult to resolve.

Case in point, the Tree of Life Web Project gives the following summary of deep branches among major animal lineages:

Each copy of the human genome consists of about 3,200,000,000 base pairs, and includes about 500,000 repeats of the LINE-1 transposable element (a LINE) and twice as many copies of Alu (a SINE), as compared to around 20,000 protein-coding genes.

Whereas protein-coding regions represent about 1.5% of the genome, about half is made up LINE-1, Alu, and other transposable element sequences. These begin as parasites, and some continue to behave as detrimental mutagens implicated in disease. However, most of those in the human genome are no longer mobile, and it is possible that many of these persist as commensal freeloaders.

Finally, it has long been expected that a significant subset of non-coding elements would be co-opted by the host and take on functional roles at the organism level, and there is increasing evidence to support this. A notable fraction of the non-genic portion of human DNA is undoubtedly involved in regulation, chromosomal function, and other important processes, but based on what we know about non-coding DNA sequences, it remains a reasonable default assumption -- though one that should continue to be tested empirically -- that much or perhaps most of it is not functional at the organism level.

This does not mean that a search for the functional segments is futile or irrelevant -- far from it, as many non-genic regions are critical for normal genomic operation and some have played an important role in many evolutionary transitions. It simply means that one must not extrapolate without warrant from discoveries involving a small fraction of sequences to the genome as a whole.