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elena-14-01-66 [18.8K]
3 years ago
12

Which object has the same shape as a DNA molecule?

Biology
1 answer:
snow_tiger [21]3 years ago
7 0
The object that has the same shape as a DNA molecule is ladder.
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a sequence of amino acids called a blank is produced during the process of blank during this process, the blank of a TRNA molecu
eduard

Answer:

A transfer RNA (abbreviated tRNA and formerly referred to as sRNA, for soluble RNA is an adaptor molecule composed of RNA, typically 76 to 90 nucleotides in length,that serves as the physical link between the mRNA and the amino acid sequence of proteins. Transfer RNA does this by carrying an amino acid to the protein synthetic machinery of a cell (ribosome) as directed by the complementary recognition of a 3-nucleotide sequence (codon) in a messenger RNA (mRNA) by a 3-nucleotide sequence (anticodon) of the tRNA. As such, tRNAs are a necessary component of translation, the biological synthesis of new proteins in accordance with the genetic code.

Each mRNA molecule is simultaneously translated by many ribosomes, all reading the mRNA from 5′ to 3′ and synthesizing the polypeptide from the N terminus to the C terminus. The complete mRNA/poly-ribosome structure is called a polysome.

tRNAs in eukaryotes

The tRNA molecules are transcribed by RNA polymerase III. Depending on the species, 40 to 60 types of tRNAs exist in the cytoplasm. Specific tRNAs bind to codons on the mRNA template and add the corresponding amino acid to the polypeptide chain. (More accurately, the growing polypeptide chain is added to each new amino acid bound in by a tRNA.)

The transfer RNAs (tRNAs) are structural RNA molecules. In eukaryotes, tRNA mole are transcribed from tRNA genes by RNA polymerase III. Depending on the species, 40 to 60 types of tRNAs exist in the cytoplasm. Serving as adaptors, specific tRNAs bind to sequences on the mRNA template and add the corresponding amino acid to the polypeptide chain. (More accurately, the growing polypeptide chain is added to each new amino acid brought in by a tRNA.) Therefore, tRNAs are the molecules that actually “translate” the language of RNA into the language of proteins.

5 0
3 years ago
In the diagram, which represents a catalyst?
KIM [24]

Answer:

where is the diagram???

4 0
3 years ago
Opsins are proteins that are found in the light-sensing cells in the human eye. Different opsin proteins are sensitive to differ
Zepler [3.9K]

Answer:

Women who carry one copy of the mutated gene still have normal color vision because they have another copy, which is not mutated, in the other X chromosome that will be the dominant one. As a result, the women are carriers of the mutated gene but not color blind.

Explanation:

Colorblindness is a sex-linked mutation. A woman has two X chromosomes, while a man has one X chromosome and one Y chromosome. The mutated gene that causes color blindness is on the X chromosome, and it is OPN1LW. So if a woman has one mutated OPN1LW in one of her two X chromosomes, the OPN1LW gene in the other X chromosome will be the dominant one stopping the woman from being colorblind.

In the case of men, as they only have one X chromosome, if there is a mutation on the OPN1LW in the X chromosome, the men will be colorblind because there is no extra copy of the gene, as it is in women.

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3 years ago
As the course of evolution has proceedin plants, what is the overall trend in the relationship of the diploid stage and the hapl
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<span>Meiosis in simple terms is the process by which gametes (sperm and egg) fuse together to produce a fertilised egg. Haploid is a word that refers to how many chromosomes a certain cell has. In this case the gametes have a haploid number of chromosomes, which is half the number a normal cell has. A normal cell has a diploid number of chromosomes. So in meiosis the two gametes come together with their hapoid number of chromosomes each to create an egg that has a diploid (standard) number of chromosomes.</span>
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Amniocentesis is a process in which amniotic fluid is taken from the mother's womb to identify any genetic abnormalities in the
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<span>B)<span>The exact location of a particular disease-causing gene can be determined.

</span></span>
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