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The human genome has many different regulatory sequences which are crucial to controlling gene expression. Conservative estimates indicate that these sequences make up 8% of the genome, [29] however extrapolations from the ENCODE project give that 20 [30] or more [31] of the genome is gene regulatory sequence.
The human genome is the total collection of genes in a human being contained in the human chromosome, composed of over three billion nucleotides. [2] In April 2003, the Human Genome Project was able to sequence all the DNA in the human genome, and to discover that the human genome was composed of around 20,000 protein coding genes.
Along with identifying all of the approximately 20,000–25,000 genes in the human genome (estimated at between 80,000 and 140,000 at the start of the project), the Human Genome Project also sought to address the ethical, legal, and social issues that were created by the onset of the project. [85]
The function of genes is to provide the information needed to make molecules called proteins in cells. [1] Cells are the smallest independent parts of organisms: the human body contains about 100 trillion cells, while very small organisms like bacteria are just a single cell.
Genes are then duplicated to form multigene families which duplicate to form superfamilies spanning multiple chromosomes. Whole genome duplication doubles the number of copies of every gene and gene family. [6] Whole genome duplication or polyploidization can be either autopolyploidization or alloploidization. Autopolyploidization is the ...
The human genome is believed to contain around 20,000–25,000 genes. In addition to studying chromosomes to the level of individual genes, genetic testing in a broader sense includes biochemical tests for the possible presence of genetic diseases, or mutant forms of genes associated with increased risk of developing genetic disorders.
How Neanderthal ancestry has shaped human genes. The research in Science found that genetic variants inherited from our Neanderthal ancestors are unevenly distributed across the human genome.
The aforementioned genome-wide association studies can identify candidate genes stemming from many functional traits. Genes can be isolated through genomic libraries and used on human cell lines or animal models to further research. [17]