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EleoNora [17]
2 years ago
6

What are the sections of dna that contain instructions for making proteins called

Biology
2 answers:
crimeas [40]2 years ago
7 0

Answer:

It is called a Gene

matrenka [14]2 years ago
3 0

Answer:

A gene

Explanation:

Each DNA sequence that contains instructions to make a protein is known as a gene.

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How do the treatments for cancer work, and why can it sometimes make people sick or weak to have them?
11111nata11111 [884]

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Most treatments for cancer use radiation to target the cancerous cells (tumor) and blast radiation in that direction. Because we cannot control the radius of the radiation, other cells are also blasted with radiation and causes sickness in cancer patients.

Explanation:

6 0
3 years ago
What's a membrane that oly lets certain particles to pass through t?
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<span>Cell Membrane which is a Selectively Permeable Membrane.

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Write an essay stating your opinion on whether pollution is a problem caused by a few or a problem caused by many?
goldenfox [79]
Does nature really hurt itself? does nature want to be ruined? if I would be a nature I will kick those people that have nothing to do but hurt me. Pollution is a result of human activities. it is a problem caused by many.
6 0
4 years ago
HELP!! DUE TODAY
goldenfox [79]

Answer:

In the past decade, genetic testing aimed at identifying ancestry has experienced exponential growth, with nearly 26 million tests sold since 2018 (6). Companies – such as 23andMe – offer kits to trace your genetic legacy and geographical origins using Y-chromosome, mitochondrial, and whole-genome markers (1). Genetic ancestry testing holds the potential to identify the geographic origins of an individual’s ancestors, ancestral lineages, and relatives, but does not define a deterministic cultural identity.

DNA located in the mitochondrion, mtDNA, is inherited maternally in both sexes and can thus provide evidence of an direct, unbroken female lineage (10). The mtDNA typically passes unchanged from mother to offspring, except in the rare case of a mutation. By comparing full mtDNA sequence or assaying for particular haplogroups, it is possible to establish both close ancestry and rough global origins, respectively (4). Regardless, two individuals, even with an exact mtDNA match, may have had an ancestor as far back as ten or sixteen generations (9). Consumers should thus be warned against over-interpreting mtDNA results since they unravel a single thread in an individual’s genetic ancestry. A distinct benefit of mtDNA tests is the ability to distinguish maternal lineage in recorded genealogical data in which females adopt the male surname (10).

Contrary to mtDNA, Y-chromosome DNA is inherited paternally, passed down from father to son. Ancestry tests analyze locations along the Y chromosome, cataloging mutations known as single nucleotide polymorphisms and repeating patterns known as short tandem repeats (8). Test results can determine if two male members of separate families with the same surname have a close genetic relationship (10). In addition, a multitude of haplogroups, representing branching in the Y-chromosome tree, can be used to examine the presence of a common ancestor thousands of years back, contributing another thread to the central question of genetic ancestry (8,7).

A more comprehensive basis of determining ancestry relies on the presence of millions of autosomal variants, such as single nucleotide variants (SNVs), across the genome (10,3,7). An individual’s unique pattern of SNVs is compared with various reference populations and other consumers in order to infer their ancestry (10). Companies such as 23andMe provide a readout of broad ancestry and specific subgroups. Ancestral populations such as European and Western Asian are often further broken down into subpopulations (e.g. British, Greek, Iran). The accuracy of more specific statistical inferences is often variable, with companies examining different SNVs reporting inconsistencies in percentages for the same individual (3). In addition, since many reference populations do not account for migration and interbreeding thousands of years back, an ethnicity estimate with a high degree of confidence could still differ drastically from an individual’s expectations (10). Statistical inferences have diminished accuracy in regions such as East Africa and South Asia with comparatively limited data relative to well studied European populations, leading to further possible inconsistencies (7).

While the commercialization of genetic-ancestry tests has resulted in improved accuracy and innovation, the hyper-aggressive marketing of such products risks misinforming consumers, particularly in regards to cultural heritage. Consider, for example, an advertisement by the company Ancestry where a woman finds “[her] strength” after realizing she shares maternal lineage to a matriarchal people in Ghana (11). The pervasive marketing has even infiltrated music: In 2018, Spotify and Ancestry partnered to suggest playlists and artists based on test results, blatantly equating DNA and cultural heritage (2). While such marketing efforts are externally harmless, they carry a hidden message that DNA plays a meaningful role in our cultural identity. Most consumers are ill-informed in the field of genomic science, and may assume that their test results are deterministic and connote a contribution to heritage.

Genetic-ancestry tests may also perpetuate the idea of innate racial differences and entangle race with culture. A randomized trial reported that White Americans with lower genetic literacy had increased essentialist views after receiving test results (6). Those of Hispanic heritage share cultural aspects such as language, but may differ in genetic test results due to post-colonial admixture of Native, European, and African populations (5). Does a test result of 90% European heritage indicate “more” Hispanic heritage than 80% African? Such conclusions are entirely inaccurate and dangerous, but plausible given the genetic literacy of the typical consumer.

Explanation:

8 0
3 years ago
Explain why most mutations in eukaryotes are recessive
Dominik [7]
There are two main reasons. First, there are introns and exons existed in eukaryotes. Introns do not contain the genetic information but are in large amount in chromosome. So, if the mutation occurs in the introns, it will be recessive. Second, one amino acid will corresponding to several base sequences. For example, UUU and UUC all represent Phe. This is called degeneracy. So if the mutation did not change the amino acid, it is also recessive.
6 0
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