Background. The early
2000s were characterized by an explosion in the number of genomes sequenced for
different species. With the preliminary annotation of the vertebrates’ genomes,
the clustered protocadherins emerged as the strongest candidates to provide
single cell identity to neurons. I decided to look at their evolution to gain insights
about their function.
Research. I showed how the
protocadherin gene clusters evolved in human and mouse after the divergence of
the species (Morgan, 2008). In particular, I found that a unique unit of evolution explains all
the recent duplication events for all the protocadherin clusters (Figure 1).
Perspective. The unit of evolution turned out to encode for the C-terminal region of a protocadherin together with the promoter region and the N-terminal region of the protocadherin immediately downstream in the cluster. Whether this form of evolution has functional implication is not known.
Perspective. The unit of evolution turned out to encode for the C-terminal region of a protocadherin together with the promoter region and the N-terminal region of the protocadherin immediately downstream in the cluster. Whether this form of evolution has functional implication is not known.
Figure 1. Evolution of part of the human b-protocadherin cluster. Each block
represents a gene. The light colored part of the gene encodes for the C-terminal
portion of the protein.
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