Preview

Lancelets

Satisfactory Essays
Open Document
Open Document
255 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Lancelets
Lancelets, also known as “Amphioxus,” are small, fishlike animals within the subphyla Cephalochordata. This organism may be tiny in size, but their impact on human evolution is tremendous! Carol MacKintosh, a professor in the College of Life Sciences at the University of Dundee, defines them as “…a very distant cousin to humans and other vertibrates. It is the creature most similar to the original spineless organism that existed before a major genomic event occurred.”

A new study indicates a genetic error, which took place 500 million years ago, led to human evolution. This organism went through two doublings of its DNA and initiated the evolution of not only various animals, but humans as well. In addition to contributing to the evolution of other organisms, this unusual event also led to proteins that are liable for several of the diseases we see today, such as diabetes and cancer. You may wonder how something like this could be discovered, and here is a little summary: MacKintosh and her research group “study a network of several hundred proteins that work inside human cells to coordinate their responses to growth factors and to insulin,” as described by Jennifer Viegas of Discovery News. A biochemical analysis of the proteins was performed, and it was discovered that they “date back to the genome duplications, which occurred during the Cambrian [Period].” Fortunately, studying these proteins can unravel and reveal additional diseases and evolution.

http://news.discovery.com/human/evolution/dna-mistake-evolution-120724.htm

You May Also Find These Documents Helpful

  • Good Essays

    cellular basis of human diseases and the role of genetics and genomics in health and disease…

    • 23814 Words
    • 82 Pages
    Good Essays
  • Satisfactory Essays

    In the article, “Elephant Genes Hold Cancer-Fighting Secret,” the author, Laura Geggel, explains how researchers have recently discovered that cancer is less common in elephants than in humans because they have more copies of a gene that stops tumor growth. Researchers that understand how this gene has evolved and why it works to stop cancer growth in elephants may be able help find ways to treat or cure cancer in humans. Researchers conducted a study that focused mainly on the TP53 gene, which normally codes for a protein that stops tumor growth. In many human cancers, this gene is mutated and unable to do its job, which allows increased cell reproduction and genomic instability. Humans inherit one copy of TP53 from each of their parents and…

    • 382 Words
    • 2 Pages
    Satisfactory Essays
  • Satisfactory Essays

    ABC Adaptations Project

    • 621 Words
    • 4 Pages

    DNA (deoxyribonucleic acid) determines who we are! If there is a mistake in coping the DNA, then it creates a mutation.…

    • 621 Words
    • 4 Pages
    Satisfactory Essays
  • Powerful Essays

    It has often been said that living things, including humans, cannot be well-understood without looking at the evolutionary forces that have shaped them. Biological science and medicine are becoming increasingly more evolutionary as our exponentially-growing knowledge base at all levels – from DNA to the process of biological inheritance; from the biology and genetics of populations and species to the evolutionary processes that shape them; from cells to multicellular beings, and from individuals to the planetary biosphere – reveals more and more clearly how living systems work.…

    • 3773 Words
    • 16 Pages
    Powerful Essays
  • Good Essays

    Blast Lab

    • 989 Words
    • 4 Pages

    The initial gene that we started with was actin and there was so many relationships between humans and other organisms. I was surprised how closely related we are to others. It showed a cladogram of the relationships.…

    • 989 Words
    • 4 Pages
    Good Essays
  • Good Essays

    Ghost in Your Genes

    • 703 Words
    • 3 Pages

    Genetic inheritance was thought to have involve the transmission of DNA from one generation to the next affected by occasional mutations in the DNA itself. They found out that the human genome was less complex and had less genes then even less complex organisms such as plants. The human genome, only containing about 30,000 genes, now lead scientists to believe that other factors allow genes to be switched on and off in response to the environment. Professor Pembrey was drawn to two genetic diseases due to families exhibiting unconventional genetic inheritance patterns. The two diseases were Angelman syndrome, which displays clinical symptoms of jerky movements, little or no speech and a very happy personality, and Prader-Willi syndrome, in which patients are found to be very floppy in infancy and develop an insatiable appetite associated with obesity in later life. He found out that these two diseases were caused by the same genetic alteration. There was a small deletion on chromosome 15. The parent from whom the mutation was inherited determined which disease the patient would get. If it was inherited from the mother the child would have Angelman syndrome and if it was inherited from the father the child would have Prader-Willi syndrome. This suggested that the chromosome knew its origin and must had been tagged or imprinted in some way. This was known as genomic imprinting. During sperm and egg production(meiosis), a chemical change results in the same DNA sequence on each chromosome having different functional properties. These events can lead to a particular gene being turned on or off. This is what epigenetics is based of. Professor Reik noticed that when a mouse embryo was placed in a culture dish some of genes would be switched off and wondered whether this could also be true for human embryos during in vitro fertilization or IVF. Using the disease, Beckwith-Wiedeman syndrome, Reik discovered that Beckwith-Wiedeman syndrome occurs…

    • 703 Words
    • 3 Pages
    Good Essays
  • Powerful Essays

    Psy 250

    • 1251 Words
    • 6 Pages

    Biology revealed many aspects of how the human body works and what it needs to stay healthy. “In 1953 James D. Watson and Francis Crick discovered that DNA was structured as a double helix (Friedman & Schustack, 2009). This discovery was a huge accomplishment in the study of human biology. Charles Darwin took human biology a step further. Darwin used the fact that not one human being is the same to support his evolutionary personality theory. Darwin believes that humans are “people evolved directly from more primitive species (Friedman & Schustack, 2009).” For example, Brian G. Richmond and David S. Strait wrote an article called “Evidence that humans evolved from a knuckle-walking ancestor (Richmond and Strait, 2000).” This article explains that evidence has surfaced proving that humans could have once been gorillas.…

    • 1251 Words
    • 6 Pages
    Powerful Essays
  • Good Essays

    Ghost In Your Genes Essay

    • 731 Words
    • 3 Pages

    “Ghost in Your Genes”- when hearing this I thought of something unknown, overtaking your body, or at least a part of your body. The movie, Ghost in Your Genes, presents an experiment done in the 1990s, called the Human Genome Project (Ghost in Your Genes). During this project, researchers were able to discover the chemical structure of each gene and overall they hoped to find a cure for all diseases, such as alzheimer's and autism (Ghost in Your Genes). It was also found out that humans, surprisingly have the same number of genes as fish and mice and chimpanzees make up 98.9% of the human genome (Ghost in Your Genes). This question then pops up- how come humans are so much more complex than these animals are? Does it have to do with something…

    • 731 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Non-coding DNA influences the activity of other genes, which could cause mutations. Due to the fact that the Human Genome Project gets bigger by the year and new information is updated almost daily, it will be easier to find any potential diseases caused by variables of the non-coding regions of the genome (Source G). The greatest genetic disturbance is caused when the “ultrasensitive” regions are altered. When major parts of the genome is not translated by the non-coding DNA, mutations occur (Source F). An international group of cancer researchers completed a study that found out that mutated non-coding DNA molecules can in fact cause cancer (Source E). A team of scientists applied a computer they developed, FunSeq, to more than 80 genomes and found approximately 100 potential non-coding cancer variants (Source G). Evidence has been found that Non-coding DNA moulds and shaped mice’s skull. The same Non-coding DNA is found in humans, and could mean that it also moulds human skulls (Source D). According to a scientist, Wray, research has shown that diseases such as bipolar and depression may be associated with mutations of the non-coding region that determines whether the brain is producing enough of a particular neurotransmitter or not (Source…

    • 556 Words
    • 3 Pages
    Good Essays
  • Better Essays

    Type 2 Diabetes Paper

    • 1400 Words
    • 6 Pages

    In the past 20 years, Type 2 diabetes has been prevalent in the United States (Eckel , Kahn, Ferranni, Goldfine, Nathan, Schwartz, & Smith, 201, p.1425). Diabetes is one of the most relevant health concerns in the U.S. Diabetes causes high rates of obesity, which may become part of a family’s history, and it can cause effects for later generations. Moreover, according to Amuta, Crosslin, Goodman, & Barry (2016), children and siblings may share up to 50% of their DNA with each other and their parents, while grandparents may share up to 25% of the genes.…

    • 1400 Words
    • 6 Pages
    Better Essays
  • Good Essays

    References: Kazan, C. Evolution May Trigger Rise of Human Disorders and Disease (2010). Retrieved on…

    • 822 Words
    • 4 Pages
    Good Essays
  • Good Essays

    Pancreas Essay

    • 1857 Words
    • 8 Pages

    “Having certain genes or combinations of genes may increase or decrease a person’s risk for developing the disease.” 14 For example, if your mother or father has diabetes you're likely to develop the onset disease. If your brother or sister has type 2 diabetes you have a 40 percent chance of developing the disease. If your identical twin has type 2 diabetes you have 100 percent chance in developing the disease. Like pre-diabetes the disease occurs more in those who are African- American, Hispanic of any race, Alaska natives, Native Americans and some…

    • 1857 Words
    • 8 Pages
    Good Essays
  • Good Essays

    The human body and DNA is so complicated and has so much to it that small things could make a big difference. Humans are made of so many cells and DNA with different functions and uses but it could all go wrong with one gene. Results of these things happening are known as disorders. From things like Down Syndrome and Heart defects. Heart defects may not seem genetic but could be passed and is a family matter, things in a family’s history can show signs.…

    • 806 Words
    • 4 Pages
    Good Essays
  • Good Essays

    The Human Genome Project

    • 958 Words
    • 4 Pages

    century and will be of great value to the field of medicine. The project will…

    • 958 Words
    • 4 Pages
    Good Essays
  • Better Essays

    Almighty Allah, due to His Mercy has given exceptional strength, talent and skill to humans and placed them at the top of Biological hierarchy. Flawless operating system of human was created by the Lord, yet genetic studies revealed that irregularities in genetic code and main control system may lead to death dealing disorders. Millions of unfortunate individuals suffering from different malformations authenticate the fact that nature has already performed extensive arbitrary mutagenesis on human brain, resulting in rich diversity of mutations that distort cortical development in distinct and surprising ways.(Walsh,1999)(70) Establishing the linkage association of genes that cause the genetic chaos, identification of the defective gene and…

    • 2604 Words
    • 11 Pages
    Better Essays