If a DNA sequence of a particular gene is 90 nucleotides long and the 31st nucleotide is deleted, then 20 amino acids would be affected by the mutation.
What is the real meaning of a mutation in a gene sequence?The real meaning of a mutation in a gene sequence is to cause any alteration that may affect the triplets of nucleotides or codons in the resulting sequence and alter the protein.
Therefore, with this data, we can see that a mutation in a gene sequence can affect the codons, and we hear 20 codons downstream.
Learn more about codons and mutations here:
https://brainly.com/question/23827103
#SPJ1
Select the correct statement about absorptiona. 30% ingested materials have been absorbed by the end of the large intestine.b. carbohydrates diffuse across the villus epithelium and are then passively transported into blood capillaries.c. if intact fats are transported across the villus epithelium, an immune response may be generated.d. Amino acid transport is linked to sodium transport.The answer could be one choice or multiple choices
The correct statement(s) about absorption is (D) Amino acid transport is linked to sodium transport.
Amino acids are transported across the villus epithelium in the small intestine, and this process is linked to sodium transport.
Amino acids, not proteins, are absorbed; proteins rely on prior digestion to amino acids. Most absorption of amino acids occurs in the jejunum; there is a lesser contribution from the ileum.
Amino acids are absorbed by a co-transport mechanism with sodium ions. Both sodium ion and amino acid combine with a cell surface protein receptor.
There are different receptors for the groups: neutral amino acids, basic amino acids, acidic amino acids
In addition, certain amino acids may have there own specific transporter e.g. proline. The receptor then conveys both molecules to the inside of the cell.
The energy for this transport is derived from the concentration gradient for sodium across the cell membrane. Na-K ATPase transporters actively and continuously pump sodium ions outwards to maintain the gradient.
To know more about absorption, refer here:
https://brainly.com/question/28196664#
#SPJ11
b1) did this change in the dna sequence cause any significant change to the protein produced? explain. b2) what is the name of this type of point mutation and why is it referred to by this terminology?
b1) No. b2). Nonsense mutation. It is same amino acid. While mutations always result in a change in the DNA sequence, they do not necessarily have noticeable impact on organism or alter resulting protein.
Since most amino acids can be encoded by two or more distinct codons, this is possible. For instance, the DNA sequences CAA and CAG both code for the amino acid valine. Hence, a valine would still be added to the protein even if the DNA sequence underwent a substitution mutation and changed from CAA to CAG.
A nonsense mutation is a type of point mutation that creates a stop/nonsense codon, thereby shutting down translation. Because doing so would result in the early production of a truncated or ineffective protein.
Learn more about amino acid here:
https://brainly.com/question/14583479
#SPJ1
Correct Translation/Transcription
DNA Strand: TAC CAT ACT
mRNA Strand: AUG GUA UGA
Identify the following as an insertion, deletion, or substitution
DNA TAC CAT ACT
mRNA AUG UUA GGA
The mRNA Strand provided (AUG GUA UGA) is not a correct transcription of the given DNA Strand (TAC CAT ACT) as it contains an insertion (U) and a substitution (G for C).
What is insertion, deletion, or substitution in Translation/Transcription?Insertion, deletion, and substitution are types of genetic mutations that can occur during the process of DNA transcription and translation.
During transcription, the DNA molecule is used as a template to synthesize an mRNA molecule. If there is a mutation in the DNA sequence, it can result in a mutation in the mRNA sequence.
Insertion occurs when an extra nucleotide is inserted into the DNA sequence, causing a shift in the reading frame. This can result in an mRNA sequence with an extra codon, which may code for a different amino acid.
Deletion occurs when a nucleotide is deleted from the DNA sequence, causing a shift in the reading frame. This can result in an mRNA sequence with a missing codon, which may also code for a different amino acid.
Substitution occurs when one nucleotide is replaced by another in the DNA sequence. This can result in an mRNA sequence with a different codon, which may code for a different amino acid.
Learn more about Translation/Transcription at: https://brainly.com/question/11214205
#SPJ1
which electron microscope technique below is used to image the surfaces of objects ranging in size from a virus to an animals head
The electron microscope technique used to image the surfaces of objects ranging in size from a virus to an animal's head is scanning electron microscopy (SEM).
Electron microscopy is a technique for imaging specimens utilizing a beam of electrons instead of visible light.
Electron microscopes can achieve much higher magnification and resolution than conventional optical microscopes because they utilize electrons instead of light.
The Scanning electron microscope (SEM) is one of the most commonly utilized types of an electron microscope. SEM is a method of imaging the surfaces of specimens utilizing an electron beam, and it is well-suited for examining a wide range of samples, from single cells ,viruses to an animal's head
It is used to study samples in a variety of scientific fields, including biology, chemistry, and physics, among others.
To learn more about the electron microscope technique :https://brainly.com/question/14149959
#SPJ11
Which of the following marrow elements provides the microenvironment for proliferation and differentiation of hematopoietic cells?A. White pulpB. Germinal centersC. Yellow marrowD. Red marrow
The marrow elements that provides the microenvironment for proliferation and differentiation of hematopoietic cells is Red marrow. The correct answer is D.
Red marrow is a soft, spongy tissue found primarily in the bone cavities of the axial skeleton and long bones. It is responsible for producing red blood cells, white blood cells, and platelets through a process called haematopoiesis.
Hematopoietic stem cells, which are responsible for producing all blood cell types, are found in the red marrow along with a variety of other cell types that contribute to the microenvironment necessary for haematopoiesis.
This includes stromal cells, which provide support and nourishment to the developing blood cells, as well as cytokines and other signaling molecules that regulate the process of proliferation and differentiation.
To know more about Red marrow, refer here:
https://brainly.com/question/819753#
#SPJ11
the epicardium is . group of answer choices also known as the parietal pericardium a layer of cardiac muscle the visceral pericardium lining the heart chambers
The epicardium is also known as the visceral pericardium. It is a layer of the heart that covers the outer surface and protects the heart muscle.
The heart and the roots of the great arteries are contained within the pericardium, also known as the pericardial sac. It consists of two layers: a serous membrane-covered interior layer and a fibrous pericardium-covered outer layer. (serous pericardium). It outlines the middle mediastinum and encloses the pericardial cavity, which is filled with pericardial fluid. It keeps the heart free from interference from other organs, shields it from illness and trauma, and lubricates the beats of the heart.
A robust fibroelastic sac called the pericardium surrounds the heart on all sides, with the exception of the bottom and the cardiac root, where the great vessels connect the heart. (where only the serous pericardium exists to cover the upper surface of the central tendon of diaphragm). While the serous pericardium is quite flexible, the fibrous pericardium is somewhat stiff. The epicardium, a continuous serous membrane invaginated onto itself as two opposite surfaces, is a covering for the heart made of the same mesothelium that makes up the serous pericardium. (over the fibrous pericardium and over the heart).
As a result, a pouch-like potential area known as the pericardial space or pericardial cavity is created around the heart, sandwiched between the two opposing serosal surfaces.
For more such questions on visceral pericardium , Visit:
https://brainly.com/question/30723885
#SPJ11
which sequence of metabolic paths could a carbon atom take to go from a molecule of glucose to a molecule of dna?
The conversion of glucose to DNA involves several metabolic pathways. A carbon atom from a molecule of glucose can take the metabolic pathways of glycolysis, pyruvate dehydrogenase, the citric acid cycle, aconitase, and thymidine synthetase to reach a molecule of DNA.
A carbon atom from a molecule of glucose can take a few different metabolic pathways to reach a molecule of DNA. First, it would have to be converted to pyruvate, a three-carbon molecule, by glycolysis. This would then be converted to Acetyl-CoA by the enzyme pyruvate dehydrogenase. Acetyl-CoA then enters the citric acid cycle, in which it combines with oxaloacetate to form citrate, a six-carbon molecule. Finally, citrate is converted to a five-carbon molecule, alpha-ketoglutarate, by the enzyme aconitase. Alpha-ketoglutarate is then converted to the four-carbon molecule succinyl-CoA, which is then converted to a molecule of DNA by the enzyme thymidine synthetase.
Learn more about glycolysis: https://brainly.com/question/737320
#SPJ11
most applications of biotechnology will come in the fields of a. all of these. b. pharmaceuticals. c. health care. d. agriculture.
Most applications of biotechnology will come in the fields of All of these. The correct option is a.
Biotechnology is a rapidly growing field of science that is used in a variety of industries, including pharmaceuticals, health care, and agriculture. Pharmaceuticals use biotechnology to develop drugs to treat diseases, health care relies on biotechnology to diagnose and treat illnesses, and agriculture benefits from biotechnology through genetic engineering, pest control, and improved crop yields.
Here you can learn more about biotechnology
https://brainly.com/question/17379372#
#SPJ11
think about where proteins are made in the cell. where are almost all amino acids in the cell? g
During translation, the mRNA, which is produced by transcription, is used as a template for the production of a particular protein. Amino acids, the building blocks of proteins, are also found in the cytoplasm of the cell.
Translation occurs in the ribosomes, which are made up of ribosomal RNA and a variety of proteins. Most amino acids are created in the cytoplasm from the breakdown of other molecules, such as glucose or fatty acids.
Amino acids are also taken up from the extracellular environment. After they are taken up, they are modified, assembled, and/or stored as necessary. The proteins produced by the ribosomes are then exported out of the cell or incorporated into other cellular structures.
Know more about Proteins here:
https://brainly.com/question/29776206
#SPJ11
extension of disc material beyond the vertebral confines with the largest measurement being that of the depth of the displaced material is best termed a
An extension of disc material beyond the vertebral confines with the largest measurement being that of the depth of the displaced material is best termed as a disc protrusion.
A disc protrusion is a spinal disc disorder in which the nucleus pulposus extrudes through the outer layer of the fibrous ring (annulus fibrosus) and protrudes into the spinal canal, either backward or sideways.
The symptoms of disc protrusion include:
Intermittent or persistent back and/or leg pain, Weakness or numbness in the limbs, Loss of bowel or bladder control (in severe cases), Pain that worsens when bending or twisting.The main causes of disc protrusion include Ageing, Poor posture, Trauma to the spine, and Repetitive strain on the spinal column from work or exercise.
Learn more about disc protrusion at https://brainly.com/question/10921401
#SPJ11
What is the difference between dominant and recessive alleles?a. Dominant alleles are the expressed form of a character, where the recessive allele ia the trait hat ia not expressed.b. Recessive alleles are always expressed, while the dominant allele is notc. Both dominant and recessive alleles are always expressed equallyd. When a dominant allele is expressed, no recessive alleles can be present
The difference between dominant and recessive alleles is that dominant alleles are the expressed form of a character, whereas the recessive allele is the trait that is not expressed.
An allele is an alternative form of a gene that occurs at the same position on a chromosome. Alleles are responsible for different traits such as hair color, eye color, and blood type.
Each individual has two alleles for each gene, one from each parent. Dominant alleles are expressed in the phenotype (physical appearance) when present in an organism's genotype (genetic makeup). It means that if an organism has at least one dominant allele, the dominant trait will be expressed.
For instance, brown eyes are dominant over blue eyes. Therefore, if an individual has a dominant allele for brown eyes, their eyes will be brown.
Recessive alleles are not expressed in the phenotype if present with a dominant allele. Recessive alleles are expressed only in homozygous individuals when there are no dominant alleles present.
For example, if an individual has a recessive allele for blue eyes and a dominant allele for brown eyes, their eyes will be brown since the dominant trait will be expressed.
Dominant and recessive alleles are inherited following the principles of Mendelian inheritance. If an individual receives two dominant alleles or one dominant and one recessive allele for a particular trait, the dominant trait will be expressed in the phenotype.
However, if an individual receives two recessive alleles for a particular trait, the recessive trait will be expressed in the phenotype.
To know more about dominant alleles, refer here:
https://brainly.com/question/14132766#
#SPJ11
how does the body decrease the blood vessel radius? how does the body decrease the blood vessel radius? vasodilation vasoconstriction cardiac muscle contraction valve closure
The body decreases the blood vessel radius by vasoconstriction.
A blood vessel is a tubular structure that transports blood throughout the body. Blood vessels are divided into three types: arteries, veins, and capillaries.
The heart pumps blood into the arteries, which then branch off into smaller arterioles that supply the capillaries.
Vasoconstriction is the process by which blood vessels constrict or narrow their diameter, increasing vascular resistance and decreasing blood flow.
It helps to control blood pressure and redirect blood flow to areas of the body that require it more urgently than other areas.
Blood vessels can constrict to various degrees, depending on the needs of the body. Vasoconstriction can be caused by a variety of factors, including hormones, drugs, and neurotransmitters.
For example, the hormone norepinephrine causes vasoconstriction by activating alpha-adrenergic receptors on the smooth muscle cells of blood vessels.
Learn more about vasoconstriction here:
https://brainly.com/question/13258282
#SPJ11
Use the codon wheel To figure out which amino acids these codon code for.
Answer:
see below
Explanation:
AUG - methionineUCC - serine CAC - histidine ACA - threonine GUU - valine UGG - tryptophan CCC - prolineGGG - glycine_______________________________________
Related information:-
Features of genetic code:-
The code is degenerate as some of the amino acids are coded by more than one codon.The code is universal, like in every organism UCC will code for serine .AUG is the start codon, it acts as initiator .UAG , UGA , UAA do not code for any amino acids thus acts as stop codon .So , in total 61 codons code for amino acids and 3 act as stop codon.________________________________________
explain in general how paracrine factors outside the cell can elicit changes in gene expression inside a cell. provide an example of a specific pathway and how it works
Paracrine factors outside the cell can cause changes in gene expression inside the cell by regulating transcription factors, which in turn regulate transcription of genes.
Transcription is the process of synthesizing RNA with the template of the genes contained in the DNA strand that occurs in the nucleus.
Here are examples of paracrine factors outside the cell that can cause changes in gene expression. An example of a specific pathway is the NF-κB signaling pathway. NF-κB is activated by paracrine factors that bind to a receptor and form a complex with an IκB protein, which is then phosphorylated by an IκB kinase, causing IκB to be released and allowing NF-κB to translocate to the nucleus and bind to the promoters of genes that regulate inflammation and cell growth.
Learn more gene expression at:
https://brainly.com/question/29791543
#SPJ11
what modification occurs to retinoblastoma that will push the cell through the restriction checkpoint?
Answer:
The modification that occurs to retinoblastoma that will push the cell through the restriction checkpoint is its phosphorylation. This allows the cell to move from G1 to S phase of the cell cycle.
What is Retinoblastoma?
Retinoblastoma is a type of cancer that grows in the retina of the eye. This cancer is one of the rarest forms of cancer and mostly affects children. The condition starts in the cells that develop into retina cells. The retina is the light-sensitive tissue located at the back of the eye.
Modification of Retinoblastoma:
The retinoblastoma protein, or pRB, regulates the progression of the cell cycle from G1 phase to S phase by binding to the transcription factor E2F. When pRB is hypophosphorylated, it prevents E2F from binding to the promoter regions of genes required for DNA replication, resulting in a G1 cell cycle arrest or checkpoint.
The phosphorylation of the RB protein enables the cell to cross the restriction checkpoint and progress from G1 to S phase of the cell cycle. This phosphorylation is carried out by the cyclin-dependent kinases (CDKs), which phosphorylate several different sites on the RB protein.
Learn more about retina here:
https://brainly.com/question/15207568#
#SPJ11
which enzyme in the photosynthetic z scheme catalyzes the pq cycle, which is analogous to complex iii and the q cycle in the mitochondrial electron transport chain?
The enzyme that catalyzes the PQ cycle in the photosynthetic Z scheme is known as the Cytochrome b₆f complex.
The PQ cycle is analogous to Complex III and the Q cycle in the mitochondrial electron transport chain. The Cytochrome b₆f complex is composed of two cytochromes, b6 and f, along with a few other cofactors.
Cytochrome b6 is a membrane-bound protein, while cytochrome f is a soluble protein. The b6f complex acts as an electron transporter, carrying electrons from plastoquinol to plastocyanin. The electrons that pass through the complex are utilized in the PQ cycle, which is responsible for the production of two molecules of ATP per electron.
So, the enzyme in the photosynthetic z scheme which is responsible for catalyzing the PQ cycle, and is analogous to complex iii and the Q cycle in the mitochondrial electron transport chain is the Cytochrome b₆f complex.
To know more about Cytochrome b₆f complex, refer here:
https://brainly.com/question/3301677#
#SPJ4
the migration of the mormons to utah would be an example of what type of genetic drift? founder effect bottleneck effect
The migration of Mormons to Utah would be an example of what type of founder effect genetic drift
What is a founder effect?Founder Effect refers to a process that occurs when a small subset of the original population becomes geographically isolated from the majority of the population.
Due to their geographic distance from the rest of the population, this subset of people breeds only among themselves, causing the frequency of certain genetic traits to be more common in this isolated population than in the larger population as a whole.In the case of the Mormon migration to Utah, the founder effect is observed.
When the Mormons first migrated to Utah, they were a small group that settled in a new area. They had limited interaction with the rest of the population, which means that genetic traits that were more common among Mormons were more common in Utah's population over time.
This is known as the founder effect.The bottleneck effect is a situation in which a significant portion of a population is destroyed, resulting in a decrease in the genetic variability of the population. In contrast, founder effect is caused by the isolation of a small group of people from the larger population.
See more about founder effect in:
https://brainly.com/question/24303618
#SPJ11
vii. explain how a single neurotransmitter can elicit different responses at different postsynaptic cells.
The neurotransmitter released by a neuron can elicit different responses at different postsynaptic cells due to different receptor proteins on the postsynaptic cell.
The receptors on the postsynaptic cell are activated by different neurotransmitters, which then cause the cell to produce different responses. For example, some receptors on the postsynaptic cell might activate certain ion channels that cause an influx of calcium ions, while others might cause an influx of sodium ions or other substances.
These different responses can be triggered by different concentrations of the same neurotransmitter, depending on the receptor proteins present on the postsynaptic cell.
Furthermore, postsynaptic cells can also have different expression levels of receptors, which can lead to different responses to the same neurotransmitter. Therefore, a single neurotransmitter can produce different responses at different postsynaptic cells depending on the types of receptors present on the cell.
To learn more about neurotransmitters, click here:
https://brainly.com/question/9725469
#SPJ11
how is the protective group removed to allow the addition of nucleotides to the probe on the dna chip
The protective group is removed to allow the addition of nucleotides to the probe on the DNA chip by: a process called Deprotection.
This process typically involves the use of a chemical or enzymatic reagent, such as hydrogen bromide, hydrazine, or an acid. The specific reagent used will depend on the type of protective group and will result in the release of the nucleotide from the protective group and the formation of an activated nucleotide ready for use.
Once the protective group has been removed, the nucleotide can be added to the probe on the DNA chip, allowing for the successful detection of the target.
To know more about reagent refer here:
https://brainly.com/question/28463799#
#SPJ11
you decide to join a lab working on osteocalcin because it works on this hormone. you know from this and the next lecture many of its functions, target organs and receptors. can you present in one page what is/are the question(s) you would want to address and how would you tackle it/them?
My approach to investigating the functions of osteocalcin would involve a combination of molecular and cellular techniques, animal models, and clinical studies, with the ultimate goal of advancing our understanding of this hormone and its potential applications in medicine.
As a researcher joining a lab working on osteocalcin, there are several questions that I would want to address in order to further our understanding of this hormone and its role in the body.
Firstly, I would want to investigate the molecular mechanisms by which osteocalcin interacts with its target organs and receptors. This could involve studying the 3D structure of osteocalcin and its binding sites, as well as using techniques such as gene expression analysis and protein-protein interaction assays to better understand how osteocalcin influences cellular signaling pathways.
Secondly, I would be interested in exploring the functional roles of osteocalcin in various physiological processes, including bone formation, glucose metabolism, and energy homeostasis. This could involve using animal models and cell culture systems to study the effects of osteocalcin on different tissues and organs, as well as conducting clinical studies to investigate the potential therapeutic applications of osteocalcin in the treatment of metabolic disorders such as diabetes.
To learn more about osteocalcin
https://brainly.com/question/30888784
#SPJ4
which term does not belong in this group? group of answer choices experiential nurture hereditary environmental
Answer:
hereditary
Explanation:
Two plants growing beside one another try to access limited available
sunlight.
What ecological interaction describes the relationship between the two
plants?
Choose 1 answers
B
Competition
Mutualism
Herbivory
Commensalism
Answer:
Competition
Explanation:
They both need sunlight but it is limited so competition rises
which of the following would not result in an increase in arterial blood pressure? group of answer choices increased blood volume increased sympathetic stimulation increased heart rate increased stroke volume increased arteriolar vasodilation
Increased arteriolar vasodilation would not result in an increase in arterial blood pressure. Vasodilation is the widening of the blood vessels, which decreases the resistance to blood flow and thus decreases arterial blood pressure. Therefore, option E, increased arteriolar vasodilation would not result in an increase in arterial blood pressure.
Increased blood volume, sympathetic stimulation, heart rate, and stroke volume all lead to an increase in arterial blood pressure by increasing cardiac output and/or resistance to blood flow. To elaborate further, an increase in blood volume increases the pressure within the cardiovascular system, while increased sympathetic stimulation increases the contractility of the heart, leading to higher cardiac output. Increased heart rate and stroke volume also lead to higher cardiac output. Conversely, vasodilation causes the opposite effect - reducing the pressure within the cardiovascular system by decreasing the resistance to blood flow.
Increased arteriolar vasodilation would not result in an increase in arterial blood pressure. Arteriolar vasodilation refers to the relaxation or widening of the arterioles, which are the small blood vessels that connect arteries and capillaries. When the arterioles dilate, they allow more blood to flow through them, which results in a decrease in blood pressure. As a result, increased arteriolar vasodilation would not result in an increase in arterial blood pressure.
To learn more about Vasodilation :
https://brainly.com/question/30715745
#SPJ11
middle portion of the small intestine that extends from the duodenum to the ileum.___
The middle portion of the small intestine that extends from the duodenum to the ileum is called the jejunum.
It is approximately 2.5 meters long and is located in the central part of the abdomen, between the duodenum and the ileum. The jejunum is responsible for the majority of nutrient absorption in the small intestine, as it contains a large surface area for absorption due to its circular folds and finger-like projections called villi.
The villi contain microvilli, which further increase the surface area for absorption. The jejunum receives partially digested food from the stomach and continues the process of digestion and absorption before passing the remaining waste to the ileum.
To learn more about duodenum refer to:
brainly.com/question/28162573
#SPJ4
What 2 things does the North Star tell us about our location? 9th grade integrated science
what are the advantages of having transcription factors to help control transcription, rather than rna polymerase alone?
Transcription is the process in which an RNA is synthesized from a strand of DNA. Transcription factors are proteins that bind to DNA in promoter regions near genes and regulate transcription by activating or repressing RNA polymerase activity.
One of the main advantages of having transcription factors is that they allow more precise regulation of gene expression. Another advantage of having transcription factors is that they allow a rapid response to environmental stimuli or cellular signals.Transcription factors are essential for precise and adaptive regulation of transcription. By enabling a rapid response to changes in the environment and cell signaling, they help ensure that genes are expressed at the right time, in the right place, and in the right amounts.
In conclusion, the presence of transcription factors allows for fine regulation of gene expression and rapid response to changing conditions in the environment and within the cell.
Lear More About Transcription factors
https://brainly.com/question/29056552
#SPJ11
why are trees found in areas of high precipitation rather than grasses? why are grasses found in drier areas?
Trees require more moisture than grasses, which is why they are found in areas of high precipitation rather than grasses. Trees are better at storing and utilizing water than grasses, so they can survive in areas with more water. Additionally, trees are able to access water deeper in the soil, allowing them to survive longer periods of drought.
Grasses, on the other hand, can survive in drier areas due to their shallow root systems. Grasses also have specialized leaves that are designed to reduce water loss, and their waxy cuticles help keep moisture in. This allows them to survive in arid environments.
In conclusion, trees require more moisture than grasses, making them better suited to areas of high precipitation, while grasses are adapted to drier climates.
Know more about precipitation here:
https://brainly.com/question/18109776
#SPJ11
Pollutants only affect specific areas and do not spread through the watershed.truefalse
False. Pollutants can affect specific areas, but they can also spread through the watershed.
Watersheds are interconnected systems where water and pollutants can flow downstream, potentially affecting many areas. Pollutants can be carried by runoff, groundwater, or atmospheric deposition, and can be transported long distances through the watershed. Additionally, some pollutants can accumulate in sediment or biota, leading to the potential for bioaccumulation and biomagnification in the food chain. Therefore, it is important to manage pollutants in watersheds on a holistic basis, taking into account the interconnected nature of these systems and the potential for pollutants to travel and impact downstream areas. Proper management practices such as source control, treatment, and monitoring can help mitigate the spread of pollutants throughout the watershed.
To know more about watershed click here:
brainly.com/question/30980611
#SPJ4
describe the specific dna changes that produce the abnormal cystic fibrosis protein (the delta f508 mutation).
The Delta F508 mutation in the CFTR gene is the most common cause of cystic fibrosis. This mutation involves a small deletion of three nucleotides (TGG) in the CFTR gene, resulting in a single point mutation. This mutation leads to the deletion of one amino acid, phenylalanine, from the CFTR protein, resulting in an inability to transport chloride ions across the cell membrane.
This deletion results in a change in the CFTR protein structure and ultimately an inability to transport chloride ions across the cell membrane. This abnormality leads to the buildup of thick, sticky mucus in the lungs and other organs, as well as other symptoms of cystic fibrosis.
In order to create this Delta F508 mutation, three nucleotides of the DNA must be deleted from the gene. Specifically, a TGG triplet must be removed from the DNA strand, resulting in a single point mutation in the CFTR gene.
Know more about cystic fibrosis here:
https://brainly.com/question/7618757
#SPJ11
which term describes an accumulation of air or gas in the pleural space that causes the lung to collapse?
The term for an accumulation of air or gas in the pleural space that causes the lung to collapse is pneumothorax.
Pneumothorax is a term that is utilized in medical language to define the development of air within the pleural space of the chest. It is also known as a collapsed lung.Air entering the pleural space via a puncture wound or as a result of an underlying illness, such as chronic obstructive pulmonary disease (COPD) or a ruptured air sac, can cause pneumothorax.
The pleural space is located between the lungs and the chest wall, and it is a thin layer filled with fluid that helps the lungs move easily during respiration. When air or gas is present in the pleural space, it can cause the lung to collapse or become compressed, reducing the amount of oxygen that can be delivered to the body's organs.
Pneumothorax is most common in tall, thin males between the ages of 20 and 40 who smoke cigarettes, according to medical research. Pneumothorax is usually treated with the insertion of a chest tube to remove the trapped air or gas and allow the lung to re-expand.
Learn more about pneumothorax here:
brainly.com/question/7158680
#SPJ11