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zubka84 [21]
3 years ago
13

Which statement describes a parasite? A parasite is beneficial to its host. A parasite is harmed in its relationship with the ho

st. A parasite only benefits when the host is alive. A parasite always kills its host and takes all the nutrients.
Biology
2 answers:
kkurt [141]3 years ago
8 0

Answer:

A paracite harms the host

Explanation:

In-s [12.5K]3 years ago
5 0

Answer:

A parasite only benefits when the host is alive.

Explanation:

You might be interested in
A plant experiences a mutation to its xylem tissue. The plant will no longer To transport
Ket [755]

Answer:

The plant will no longer be able to transport water and dissolved minerals from the roots to the rest of the plant

6 0
2 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
2 years ago
One language used for scientific naming
julia-pushkina [17]
Latin I think. It's like nomenclature, or something like that. ☺
6 0
3 years ago
Please help i need to turn this in
makvit [3.9K]

Answer:

Normal Strand: alanine - methionine - histidine
Mutated Strand: glutamine - cysteine - no third amino acid.

Explanation:

<h3>mRNA Structure</h3>

Messenger ribonucleic acid (mRNA) is the RNA that is used in cells for protein synthesis. It has a single strand made by the transcription of DNA by RNA polymerase. It contains four nucleotides: Adenine (A), Guanine (G), Cytosine (C), and Uracil (U).

<h3>DNA Replication</h3>

Before transcribing, we need to create the complementary strand of the DNA. We're going to write out the nucleotides of the complementary strand by matching the nucleotides in these pairs: (A & T) and (C & G).

              Normal Strand: GCA ATG CAC
Complementary Strand: CGT TAC GTG

Next, we can transcribe this to find our mRNA. We're going to do the same thing to the complementary DNA strand, but with Uracils instead of Thymines. So our pairs are: (A & U) and (C & G)

Complementary DNA Strand: CGT TAC GTG
                        mRNA Strand: GCA AUG CAC

You'll notice that the mRNA strand is almost exactly like the new mRNA strand, but with Uracil instead of Thymine.

<h3>Reading Codons</h3>

Each set of three nucleotides is known as a codon, which encodes the amino acids that ribosomes make into proteins. To read the codons, you need to have a chart like the one I attached. Start in the middle and work your way to the edge of the circle. Some amino acids have multiple codons. There are also "stop" and "start" codons that signify the beginning and ends of proteins.

mRNA Strand: GCA AUG CAC
Amino Acids:   Ala   Met   His

Our sequence is alanine, methionine, and histidine.

<h3>Frameshift Mutations</h3>

A frameshift mutation occurs when a nucleotide is either added or removed from the DNA. It causes your reading frame to shift and will mess up every codon past where the mutation was. This is different than a point mutation, where a nucleotide is <em>swapped</em> because that will only mess up the one codon that it happened in. Frameshift mutations are usually more detrimental than point mutations because they cause wider spread damage.

<h3>Mutated Strand</h3>

Let's repeat what we did earlier on the mutated strand to see what changed.

              Mutated Strand: CAA TGC AC
Complementary Strand: GTT ACG TG
---
Complementary DNA Strand: GTT ACG TG
                        mRNA Strand: CAA UGC AC
---
mRNA Strand: CAA UGC AC
Amino Acids:   Glu   Cys   X
---
Our amino acid sequence is glutamine, cysteine, and no third amino acid.

As you can see, removing the first nucleotide of the strand caused every codon to change. The last codon is now incomplete and won't be read at all. If this happened in a cell, the protein that was created from this mutated strand would be incorrect and may not function completely or at all.

5 0
1 year ago
Read 2 more answers
4. The diagram below represents one possible immune response that can occur in the human body.
krek1111 [17]

Answer:

A and C only

Explanation:

I'm sorry I don't know how to explain it but trust me its A and C only.

8 0
2 years ago
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