期刊
TRENDS IN GENETICS
卷 19, 期 4, 页码 207-216出版社
ELSEVIER SCIENCE LONDON
DOI: 10.1016/S0168-9525(03)00054-4
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资金
- NCRR NIH HHS [S10 RR015934-01, RR15934] Funding Source: Medline
- NIAID NIH HHS [R21 AI058789, R21 AI054369] Funding Source: Medline
- NIDDK NIH HHS [R01 DK043739, DK43739] Funding Source: Medline
- NIGMS NIH HHS [R01 GM063162, GM63162] Funding Source: Medline
- NINDS NIH HHS [R21 NS067671] Funding Source: Medline
Alteration of mRNA sequence through base modification mRNA editing frequently generates protein diversity. Several proteins have been identified as being similar to C-to-U mRNA editing enzymes based on their structural domains and the occurrence of a catalytic domain characteristic of cytidine deaminases. In light of the hypothesis that these proteins might represent novel mRNA editing systems that could affect proteome diversity, we consider their structure, expression and relevance to biomedically significant processes or pathologies.
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