 |
Published by
 Australian Academy of Science
|

|
Biology meets industry genomics, proteomics, phenomics
Box 1 | Unveiling the proteome
|
If sequencing the human genome was a massive undertaking, consider some of the challenges
involved in creating a map of the human proteome:
Firstly, there are far more proteins in an organism than there are genes. Part of the reason for
this is that messenger RNA (mRNA), the mobile copy of DNA which is used as a template when a
cell creates a protein, can undergo 'editing' after it is first copied.
Segments of the RNA can be removed before a protein is created from it, meaning
a number of different proteins can be created from the same gene. Even after
the protein has been translated from the mRNA it can still undergo numerous
transformations including the addition of chemical groups, the removal of
sections of the protein, and combination with other proteins any of which can
alter the form and function of the finished molecule. An extreme example is a
fruit fly gene which was discovered by scientists to code for 38,000 different
proteins! So while we now know that humans have approximately 30,000 genes, our
total number of proteins is still unknown although estimates put the total at
100,000 or more.
Secondly, while the genome remains relatively static in any given cell in an organism, the
expression of the proteome changes from cell to cell and from moment to moment.
Age, gender, health, and recent consumption of food or drugs all affect the
proteome the same cell, if examined at different times or under different
conditions, can be expressing a different complement of proteins.
Thirdly, cells from different tissues within the same organism express distinct sets of
proteins.
These and other
factors involved in making a map of the human proteome present a challenge
worthy of the potential rewards it might offer.
Related sites
Other boxes
Box 2. Case study Remicade and Glivec
|





|