27.12.2014 Views

4 - Central Institute of Brackishwater Aquaculture

4 - Central Institute of Brackishwater Aquaculture

4 - Central Institute of Brackishwater Aquaculture

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

Nattonal Workshop-cum-Tra~ning on Bioinfam.ti& and Information Management in <strong>Aquaculture</strong><br />

Internet database resource:<br />

htt~://www,meddb,info/index.~h~.encat=8<br />

htt~://~~~.ebi.ac.uk/2can/da~ses/dna.html<br />

htt~://www.ebi.ac.uk/2can/databases/aenomic.html<br />

http://www.ebi.ac.uk/2can/databases/bib.html<br />

3. Transcrlptomics<br />

Expression <strong>of</strong> a biological trait in an organism is linked to the function <strong>of</strong> one or<br />

combination <strong>of</strong> few genes. Alternatively, it may be said that genes express the<br />

biological traits <strong>of</strong> humans, animals, plants and microorganisms. The acquisition<br />

<strong>of</strong> new knowledge about genes will make it possible to identify, prevent or treat<br />

disease in humans, animals and plants. Using new technology, it is possible to<br />

study tens <strong>of</strong> thousands <strong>of</strong> genes at once. Thus it has become a realistic<br />

objective to determine how the genes in an organism function. At the messenger<br />

RNA level, above 5 million ESTs (expressed sequence tags) <strong>of</strong> the<br />

complementary DNAs (cDNAs) <strong>of</strong> messenger RNAs have been sequenced in<br />

humans. In plants, several millions have been sequenced in soyabean, maize,<br />

tomato and Arabidopsis.. These sequences can be used to create high-density<br />

filters, DNA chips or microarrays, where thousands <strong>of</strong> cDNAs are fixed on a small<br />

surface, which is then hybridized with the mRNAs from a given stage or organ. It<br />

can thus be answered which genes among thousands are expressed in a<br />

particular cell type <strong>of</strong> an organism, at a particular time and stage. Such<br />

transcriptomics tools will soon permit extensive study <strong>of</strong> transcription and its<br />

regulation.<br />

Database Resource:<br />

1. htt~://www.ncbi.nlm.nih.aov/dbEST<br />

2. http://www.ebi.ac.uk/2can/databases/microarray.html<br />

4. Proteomics<br />

Most genes code for and work through proteins. Proteins may have a wide<br />

variety <strong>of</strong> functions in an organism. Thus it is <strong>of</strong> great significance to know how<br />

proteins function. The complete pr<strong>of</strong>ile <strong>of</strong> proteins expressed in a cell is called<br />

the cell's proteome. There are thousands <strong>of</strong> different proteins in each individual<br />

cell, and different types <strong>of</strong> cells contain different sets <strong>of</strong> proteins. The objective<br />

<strong>of</strong> proteomics is to discover how these proteins function and interact with one<br />

another. In order to determine the effect <strong>of</strong> proteins, it is necessary to know<br />

their composition; i.e., the way in which their components are arranged. It is<br />

also necessary to know the form that they take, i.e., their three-dimensional<br />

structure. Most proteins are coiled in a particular way and can only fulfill their<br />

function if they assume the correct three-dimensional structure. Techniques have<br />

been developed for visual imaging <strong>of</strong> proteins, but determining protein structures<br />

is technically demanding. Data have been stored for a couple <strong>of</strong> thousand<br />

different protein structures in international databases, but the three-dimensional<br />

structure for most <strong>of</strong> the proteins has not yet been determined. In many cases<br />

only parts <strong>of</strong> these proteins' structures have been determined, perhaps only the<br />

biologically active part.

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!