Cell proliferation is a regulated process. The major events that determine production of new cells, from growth factors stimulation to cell division, are briefly summarized. Regulation of cell growth is exerted on specific cell cycle events. It depends upon specially evolved biochemical mechanisms,
Proteomics and regulomics: The yin and yang of functional genomics
✍ Scribed by Thomas Werner
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 232 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0277-7037
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
| I. | Introduction | 25 |
| | A. A Brief History of Computer Application in Protein Sequence Analysis | 25 |
| | B. Requirements of Current Proteomics Research | 26 |
| | C. Mass Spectrometry Applications in Proteomics | 26 |
| II. | Basics of Transcriptional Regulation | 26 |
| | A. How Is Transcriptional Coregulation Achieved? | 26 |
| | B. Promoters and Transcription Complexes | 27 |
| III. | Synergisms Between Gene Regulation and Mass Spectrometry‐Based Proteomics | 29 |
| | A. Expression Array‐Based Gene Selection | 29 |
| | B. Protein Data‐Driven Coregulation Analysis | 30 |
| | C. A Practical Application Example | 30 |
| IV. | Conclusions | 30 |
| Acknowledgments | 32 |
| References | 32 |
Protein analysis is a field of research with a long history. Recently, the development of a series of proteomics approaches, i.e., simultaneous analyses on all or a majority of proteins in a cell at a given state, has reinvigorated protein analyses. Mass Spectrometry also developed into one of the most versatile technical tools supporting or even enabling many proteomics‐oriented approaches, providing a convenient link between experimental protein analysis and the corresponding amino acid sequences. Thus direct links to the genomic sequence can be established, which opens the door for a synergistic combination with genomic sequence analysis. This review focuses especially on aspects of genome‐wide transcription control, regulomics in analogy to all the other ‐omics, and how a combination of MS‐based proteomics with in silico regulomics analyses can produce synergistic effects in the quest to understand how cells function. This is illustrated on a real life example showing how the MS‐analysis and in silico promoter analysis can extend the list of candidates for signaling pathways, here the MAP kinase pathway. © 2003 Wiley Periodicals, Inc., Mass Spec Rev 23:25–33, 2004
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