The Case for an Early Biological Origin of DNA

被引:18
|
作者
Poole, Anthony M. [1 ,2 ]
Horinouchi, Nobuyuki [3 ]
Catchpole, Ryan J. [1 ]
Si, Dayong [3 ,4 ]
Hibi, Makoto [3 ]
Tanaka, Koichi [3 ]
Ogawa, Jun [3 ]
机构
[1] Univ Canterbury, Sch Biol Sci, Biomol Interact Ctr, Christchurch 8140, New Zealand
[2] Univ Canterbury, Allan Wilson Ctr, Christchurch 8140, New Zealand
[3] Kyoto Univ, Grad Sch Agr, Div Appl Life Sci, Sakyo Ku, Kyoto 6068502, Japan
[4] Univ Hawaii, Dept Mol Biosci & Bioengn, Honolulu, HI 96822 USA
基金
日本学术振兴会;
关键词
Ribonucleotide reductase; Deoxyriboaldolase; Last Universal Common Ancestor; RNA world; DNA origins; UNIVERSAL COMMON ANCESTOR; DEPENDENT RNA-POLYMERASE; RIBONUCLEOTIDE REDUCTASE; CRYSTAL-STRUCTURE; 2-DEOXYRIBOSE; 5-PHOSPHATE; REPLICATION MACHINERIES; ESCHERICHIA-COLI; GENETIC-CODE; DOMAINS; EVOLUTION;
D O I
10.1007/s00239-014-9656-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
All life generates deoxyribonucleotides, the building blocks of DNA, via ribonucleotide reductases (RNRs). The complexity of this reaction suggests it did not evolve until well after the advent of templated protein synthesis, which in turn suggests DNA evolved later than both RNA and templated protein synthesis. However, deoxyribonucleotides may have first been synthesised via an alternative, chemically simpler route-the reversal of the deoxyriboaldolase (DERA) step in deoxyribonucleotide salvage. In light of recent work demonstrating that this reaction can drive synthesis of deoxyribonucleosides, we consider what pressures early adoption of this pathway would have placed on cell metabolism. This in turn provides a rationale for the replacement of DERA-dependent DNA production by RNR-dependent production.
引用
收藏
页码:204 / 212
页数:9
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