DNA sequencing and assembly. Cost of sequencing. (pp. 116-118)
Annotators interpret the genomeDNA sequences are depositied in GenBank. The gene for triose phosphate isomerase (TPI1) is a typical gene. Decoding a protein-coding gene. (pp. 118-122)
How much of the genome has been sequenced?Human annotators must interpret the DNA sequence. (pp. 122-123) [ Contaminated genome sequences]
About 95% of the genome has been sequenced in the standard reference genome. The rest is estimated from the size of the gaps giving a total of 3.1 Gb. The complete telomere-telomere sequence of T2T-CHM13 is also 3.1 Gb. (pp. 123-125) [Karen Miga and the telomere-to-telomere consortium] [A complete human genome sequence (2022)] [What do we do with two different human genome reference sequences?] [How big is the human genome (2023)?]
The Celera sequence was mostly Craig Venter's genome. The IHGP standard reference genome was originally a composite of several difference individuals from Buffalo (New York, USA). (pp. 125-126)How many genes?
PseudogenesThe original genome sequence predicted 30,000-40,000 protein-coding genes but that number has dropped to about 20,000 in the current standard reference genome. There are about 5,000 noncoding genes but this number is disputed. Introns take up most of a protein-coding gene and introns are mostly junk DNA. (pp. 126-128) [Are introns mostly junk?]
There are abot 15,000 pseudogenes derived from protein-coding genes. The number derived from noncoding genes is not known. Pseudogenes account for about 5% of the genome. (p. 128)Regulatory sequences
If we assume about 200 bp of regulatory sequence for each gene then regulatory sequences account for less than 0.2% of your genome. Many scientists believe this number should be much higher. (pp. 128-129)Origins of replication
There are about 30,000-50, 000 functioning origins of replication accounting for <0.3% of your genome. (pp. 129-130)Centromeres
About 1% of your genome is occupied by centromeres. (p. 130) [Centromere DNA] [Minimum Centromere Size in Plants]Telomeres
Telomere sequences are about 0.1%. (pp. 130-131) [Telomeres]Scaffold Attachment regions (SARs)
SARs are required for chromatin organizaton and it's not clear how much DNA sequence is required. Assuming 100,000 loops and 100 bp of SAR per loop gives 0.3% of the genome. (p. 131)Transposons
About 55% of the genome contains transposon-related and virus-related sequences. They are scattered throughout the genome including within introns. (pp. 131-132)Viruses
Defective viruses take up about 9% of the genome and functional, dormant, viruses account for less than 0.1%. (p. 132)Mitochondrial DNA
Less than 0.01% of your genome is occupied by mitochondrial DNA fragments. (p. 132)How much of our genome is functional?
Adding up all the known functional sequences gives a value of about 4% functional. The actual amount is probably closer to 8-10% based on sequence conservation. The total amount of presumed junk DNA comes to 89%. About 90% of your genome is junk. (pp. 132-133) [The 20th anniversary of the human genome sequence: 4. Functional DNA in our genome]
Junk DNA is DNA that can be deleted without reducing the fitness of the individual. The debate is not whether junk DNA exists (it does) but over the amount of junk DNA. Opponents of junk DNA think that it would have been eliminated by natural selection if it were really junk. This is a common view in the popular press and even in the scientific literature. My vew is that genomes are sloppy and natural selection isn't capable of purging junk DNA in species with large genomes. (pp. 133-135) [Identifying functional DNA (and junk) by purifying selection]Notes for Chapter 5 (p. 324)
