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Genomic streamlining

The Human Genome Project went three-dimensional in late 2000. Structural genomics efforts will determine the structures of thousands of new proteins over the next decade. These initiatives seek to streamline and automate every experimental and computational aspect of the structural determination pipeline, with most of the steps involved covered in previous chapters of this volume. At the end of the pipeline, an atomic model is built and iteratively refined to best fit the observed data. The final atomic model, after careful analysis, is deposited in the Protein Data Bank, or PDB (Berman et ah, 2000). About 25,000 unique protein sequences are currently in the PDB. High-throughput and conventional methods will dramatically increase this number and it is crucial that these new structures be of the highest quality (Chandonia and Brenner, 2006). [Pg.191]

Automated carbohydrate synthesis allows for the production of complex carbohydrates orders of magnitude faster than other approaches. This advance has the potential to parallel the breakthroughs achieved by researchers in the peptide and DNA fields that opened up the pro-teomic and genomic eras in biotechnology. By increasing the scope of the carbohydrate building block library and streamlining the reaction conditions further we anticipate that automated solid-phase carbohydrate synthesis will become the method of choice for carbohydrate production. [Pg.243]

Should development come after speciation Yes, of course, in the new model it is natural, one produces the Anlage and develops it to its potential. The word evolution is derived from the latin term evolvere which means to roll out and that describes precisely the process postulated in the Genomic Potential Hypothesis for the post-Cambrian time. With speciation behind us there remain two distinct ph ases of evolution in the widest sense of the word, the streamlining of the chemistry in the nucleus, which leaves no traces other than species-specific stem cells, and the post-Cambrian unrolling of species and variants that produces a spectacular display of phenotypes. Looks like we are on the right track. [Pg.51]

If the first cells had genomes that contained both functional and junk RNAs, they also had before them two different evolutionary strategies one was to get rid of the junk RNAs, the other was to keep them. The first strategy led to a generalised streamlining, and was embraced by those cells that eventually became bacteria. The... [Pg.183]

As we can see, it is far too early to draw reliable conclusions about eukaryotic genomes, but once again we can appreciate how important it is to distinguish between simple and primitive properties. The streamlining strategy did succeed in producing cells that combined maximum efficiency and maximum simplicity, but when all that was erasable was in fact erased, it become impossible to go further, and bacterial evolution reached a sort of stationary state. Other cells, instead, went on with primitive cargoes and junk molecules, and their evolution remained open, free, creative and unpredictable. [Pg.184]

From this, in Forterre s thermoreduction hypothesis (1995), came several lines of descendants. Some became colonists of much hotter environments. Of these lines, some necessarily streamlined both their genomes and their physiology, in order to survive, while others, also with reduced physiology, developed heat shock proteins to correct damage. This led to the distinct domains, the Bacteria and Archea. In contrast, other descendants retained the complex more primitive physiology— biplanes or triplanes, as opposed to prokaryote monoplanes. This third line became the Eucarya. This third line may share some characteristics with the planctomycetes (Fuerst, 1995 Lindsay et al, 2001). [Pg.3900]

The streamlined setting of the Array-On platform is very well suited for rapid and high-throughput SNP analyses. Blackouts are only observed in PCR-based sample amplification, due to genomic primer site mutations that prevent correct binding of the PCR primers to the sample DNA. Only in these cases can no PCR product be observed and used for primer extension. Primer extension will perform well, as... [Pg.106]


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See also in sourсe #XX -- [ Pg.53 ]




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