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The problem of multiple comparisons received increased attention in the 1950s with the work of statisticians such as Tukey and Scheffé. Over the ensuing decades, many procedures were developed to address the problem. In 1996, the first international conference on multiple comparison procedures took place in Tel Aviv. [3]
A typical replication origin covers about 100-200 base pairs of DNA. Prokaryotes have one origin of replication per chromosome or plasmid but there are usually multiple origins in eukaryotic chromosomes. The human genome contains about 100,000 origins of replication representing about 0.3% of the genome. [25] [26] [27]
For eukaryotic chromosomes, there are multiple replicons per chromosome. Known examples range in size from 10 to 330 kilobases. A cluster of replicons replicates simultaneously. But different clusters start replicating at different times during S phase, depending on their location along the chromosomes
The genomes of most eukaryotic mitochondria and plastids are in a single circular chromosome, in line with their bacterial ancestor. However, a good number of eukaryotic species do harbor linear Mitochondrial DNA (mtDNA), some even broken into multiple molecules, across a wide variety of taxa: animals (mammals, medusozoans, sponges), fungi (especially yeast), plants, and Alveolatas.
There are two types of plasmid integration into a host bacteria: Non-integrating plasmids replicate as with the top instance, whereas episomes, the lower example, can integrate into the host chromosome. In order for plasmids to replicate independently within a cell, they must possess a stretch of DNA that can act as an origin of replication.
Additionally, nitrous acid (HNO2) is a potent mutagen that acts on replicating and non-replicating DNA. It can cause deamination of the amino groups of adenine, guanine and cytosine. Adenine is deaminated to hypoxanthine, which base pairs to cytosine instead of thymine. Cytosine is deaminated to uracil, which base pairs with adenine instead of ...
Differentiated somatic cells of adult mammals generally replicate infrequently or not at all. Such cells, including, for example, brain neurons and muscle myocytes, have little or no cell turnover. Non-replicating cells do not generally generate mutations due to DNA damage-induced errors of replication.
This is based on the fact that viral agents are simple particles or molecules that replicate and are transferred between various hosts like the remaining non-viral mobile genetic elements. According to this point of view, viruses and other viral agents should not be considered living beings and should be better conceived as mobile genetic elements.