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nadezda [96]
3 years ago
9

59:10 A chemical has been found to harm the same components in both prokaryotic and eukaryotic cells. Which components are those

? DNA, cell membrane, cytoplasm, and ribosomes DNA, cell membrane, ribosomes, and membrane-bound organelles DNA, cytoplasm, ribosomes, and nucleus DNA, cell membrane, cytoplasm, and membrane-bound organelles
Biology
2 answers:
kotykmax [81]3 years ago
8 0

Answer:

DNA, cell membrane, cytoplasm, and ribosomes.

Explanation:

MrMuchimi3 years ago
7 0
DNA, cell membrane, cytoplasm, and ribosomes.

Both prokaryotic and eukaryotic cells have structures in common. All cells have a cell membrane, ribosomes, cytoplasm, and DNA. The cell membrane, or plasma membrane, is the phospholipid layer that surrounds the cell and protects it from the outside environment.

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6) If a mutation happens in a cancer-causing gene to change the subsequent protein's function,
Aneli [31]

Explanation:

B) False

Multiple mutations in several protooncogenes and tumor suppressor genes are required to form cancer

Cancer-causing genes, or oncogenes, develop from protooncogenes which regulate normal cell division. They may undergo mutations that alter gene expression, disrupt cell regulation and lead to the transformation of normal cells into tumor cells- their resulting proteins are abnormal or not formed. Tumor suppressor genes, which can halt unregulated cell growth and division, may also become mutated.

Each individual inherits 2 copies of a gene from their parents- a single mutation in one of these does not directly lead to cancer. Multiple activated oncogenes, in turn produce damaged, non functional proteins and together contribute to forming cancers.

Further Explanation:

During the process of cell division, spontaneous changes within the genome can arise. These mutations are errors occur when copies of the DNA within the cell are made; mutations may range from small changes called single nucleotide polymorphisms, to large scale deletions, and additions which span multiple genes. There are two types:

  • somatic: these only occur within certain cells, and arise from environmental factors such as UV light
  • hereditary: occur within germ cells of the parent and later the fertilized egg which forms a zygote; these are present within all cells of the new organism.

Sequences of DNA make up genes which can have different forms called alleles. DNA, which makes up the genotype, is transcribed into mRNA and later translated into amino acids which are linked together by rRNA to form proteins which make up the phenotype of an organism. Mutations in DNA sequences affect the corresponding mRNA and thus the protein encoded.

Learn more about mutations at brainly.com/question/4602376

Learn more about DNA and RNA at brainly.com/question/2416343?source=aid8411316

#LearnWithBrainly  

6 0
3 years ago
Kelly is concerned about the growth of her premature daughter quinn. at quinn's last pediatrician appointment, the doctor assure
HACTEHA [7]
For the answer to the question above, the <span>head circumference is a means of assessing brain growth.

It means that even though her daughter is premature. She's growing normally and without any brain problem or whatsoever and she's healthy.

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8 0
3 years ago
Read 2 more answers
Which hormone released by the highlighted structure inhibits the secretion of fsh only inhibin?
qwelly [4]

Inhibin hormone released by the highlighted structure inhibits the secretion of FSH only.

<h3>What is inhibin hormone?</h3>
  • A protein called inhibin is secreted by the granulosa cells in women and the Sertoli cells in men.
  • It decreases the amount of LH-releasing hormone in the hypothalamus and prevents the pituitary gland from producing and releasing follicle-stimulating hormone.
  • Inhibin is a factor in the feedback control of FSH secretion in both males and females going through puberty.
  • Follistatin suppresses FSH-subunit expression like inhibin, whereas activin enhances it, which in turn influences FSH production and secretion.
  • Inhibin A is secreted by the corpora lutea and dominant ovarian follicles in women, which helps to explain why levels are so high during the late follicular and luteal stages.
  • During the late luteal and early follicular phases of the menstrual cycle, inhibin B is reciprocally raised.

Learn more about inhibin here:

brainly.com/question/17257108

#SPJ4

Disclaimer: The question given in the portal is incomplete. Here, The complete question.

Question: Which hormone released by the highlighted structure inhibits the secretion of FSH only?

5 0
1 year ago
Prader-Willi syndrome is a genetic disorder involving a partial deletion of chromosome 15q on the paternal chromosome. When both
Kay [80]

Answer:

genomic imprinting

Explanation:

Genomic imprinting is a mechanism for regulating gene expression that allows expression of only one of the parental alleles, although both alleles are functional. Unlike most genes in which expression is biallelic, genes that are subjected to this mechanism (imprinted genes) have monoalelic expression; By definition, in an imprinted loci, only one allele is active (maternal or paternal), and the inactive is epigenetically marked by histonic modification and / or methylation of cytosines.

Genomic imprinting can cause some disturbances, among them Prader-Willi syndrome, which is a genetic disorder that involves a partial deletion of chromosome 15q on the paternal chromosome.

3 0
3 years ago
Genes that control hair or feather color in some animals are expressed differently in the winter than in the summer. How might s
Delicious77 [7]
In the winter its color changes to more resemble their <em>winter</em> surroundings, so they are more white, enabling them to blend in better with their white surroundings. In summer, its color changes to more resemble its <u><em /></u><em>summer</em> surroundings, so they are more brown like the rocks and ground around them.
8 0
2 years ago
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