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Marrrta [24]
3 years ago
15

A template dna strand contains the sequence 5'-atgctgac-3'. the corresponding sequence in the rna transcript is:

Biology
1 answer:
scoundrel [369]3 years ago
7 0
<span>5'-GUCAGCAU-3'. is your answer</span>
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What causes amino acids to fold in different patterns to form different looking structures?
True [87]

Answer:

Hydrogen bonding

Explanation:

Hydrogen bonding causes folding in different patterns of amino acids. This folding is responsible for the formation of different structures of proteins. This folding also helps in producing the secondary structure of protein. This hydrogen bond is present between amino groups and carboxyl groups which helps them in folding their structure in different patterns.

4 0
3 years ago
I
natka813 [3]

Answer:

When a genetic disorder is diagnosed in a family, family members often want to know the likelihood that they or their children will develop the condition. This can be difficult to predict in some cases because many factors influence a person's chances of developing a genetic condition. One important factor is how the condition is inherited. For example:

Autosomal dominant inheritance: A person affected by an autosomal dominant disorder has a 50 percent chance of passing the mutated gene to each child. The chance that a child will not inherit the mutated gene is also 50 percent. However, in some cases an autosomal dominant disorder results from a new (de novo) mutation that occurs during the formation of egg or sperm cells or early in embryonic development. In these cases, the child's parents are unaffected, but the child may pass on the condition to his or her own children.

Autosomal recessive inheritance: Two unaffected people who each carry one copy of the mutated gene for an autosomal recessive disorder (carriers) have a 25 percent chance with each pregnancy of having a child affected by the disorder. The chance with each pregnancy of having an unaffected child who is a carrier of the disorder is 50 percent, and the chance that a child will not have the disorder and will not be a carrier is 25 percent.

X-linked dominant inheritance: The chance of passing on an X-linked dominant condition differs between men and women because men have one X chromosome and one Y chromosome, while women have two X chromosomes. A man passes on his Y chromosome to all of his sons and his X chromosome to all of his daughters. Therefore, the sons of a man with an X-linked dominant disorder will not be affected, but all of his daughters will inherit the condition. A woman passes on one or the other of her X chromosomes to each child. Therefore, a woman with an X-linked dominant disorder has a 50 percent chance of having an affected daughter or son with each pregnancy.

X-linked recessive inheritance: Because of the difference in sex chromosomes, the probability of passing on an X-linked recessive disorder also differs between men and women. The sons of a man with an X-linked recessive disorder will not be affected, and his daughters will carry one copy of the mutated gene. With each pregnancy, a woman who carries an X-linked recessive disorder has a 50 percent chance of having sons who are affected and a 50 percent chance of having daughters who carry one copy of the mutated gene.

Y-linked inheritance: Because only males have a Y chromosome, only males can be affected by and pass on Y-linked disorders. All sons of a man with a Y-linked disorder will inherit the condition from their father.

Codominant inheritance: In codominant inheritance, each parent contributes a different version of a particular gene, and both versions influence the resulting genetic trait. The chance of developing a genetic condition with codominant inheritance, and the characteristic features of that condition, depend on which versions of the gene are passed from parents to their child.

Mitochondrial inheritance: Mitochondria, which are the energy-producing centers inside cells, each contain a small amount of DNA. Disorders with mitochondrial inheritance result from mutations in mitochondrial DNA. Although these disorders can affect both males and females, only females can pass mutations in mitochondrial DNA to their children. A woman with a disorder caused by changes in mitochondrial DNA will pass the mutation to all of her daughters and sons, but the children of a man with such a disorder will not inherit the mutation.

It is important to note that the chance of passing on a genetic condition applies equally to each pregnancy. For example, if a couple has a child with an autosomal recessive disorder, the chance of having another child with the disorder is still 25 percent (or 1 in 4). Having one child with a disorder does not “protect” future children from inheriting the condition. Conversely, having a child without the condition does not mean that future children will definitely be affected.

Although the chances of inheriting a genetic condition appear straightforward, factors such as a person's family history and the results of genetic testing can sometimes modify those chances. In addition, some people with a disease-causing mutation never develop any health problems or may experience only mild symptoms of the disorder. If a disease that runs in a family does not have a clear-cut inheritance pattern, predicting the likelihood that a person will develop the condition can be particularly difficult.

Estimating the chance of developing or passing on a genetic disorder can be complex. Genetics professionals can help people understand these chances and help them make informed decisions about their health.

7 0
3 years ago
Deb is studying the difference between 2 types of soil. She notices that her plants grow more when they have additional nitrogen
Dennis_Churaev [7]

The molecule, which the plant is most likely synthesizing using the extra nitrogen is PROTEIN.

Plants and animals do not have the capacity to use atmospheric nitrogen as nutrient. Atmospheric nitrogen has to be converted to forms that are usable by plants and animals before they can utilize it. Nitrogen fixing bacteria are the ones that are responsible for converting atmospheric nitrogen to the forms such as nitrate and ammonium, which can be used by plants. Animals get their own portion of nitrogen when they eat plants or other animals. Nitrate is the form of nitrogen that is mostly used by plants. Excess ammonium in plants are usually used directly to synthesize proteins. Nitrogen is a very important component of chlorophyll, which is essential for photosynthesis. Nitrogen is also found in the genetic materials of plants and it is needed for their growth and development.  Animals used nitrogen to synthesize proteins, nucleic acid and other biological compounds that contain nitrogen.

3 0
3 years ago
All BUT one factor contributes to biological evolution. That is
eduard

A. The answer is Mitosis

please rate my answer

4 0
3 years ago
Which is a consumer? *<br> Grass<br> Tree<br> Snake
Masja [62]
A snake, as it eats other meat, not plants.
7 0
3 years ago
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