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sertanlavr [38]
3 years ago
5

Which organization negotiates trade agreements, settles disputes, and enforces compliance among member nations? A. European Unio

n B. NAFTA C. World Trade Organization D. World Bank
Biology
1 answer:
mixas84 [53]3 years ago
5 0
<u>C </u>Would Be The Correct Answer!

:)
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According to the pedigree chart, which statement MUST be true?
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B

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This is because the original male is not affected by the disease. In the second generation they have a female child who is a carrier of the disease because she passes it down to her son, but she is not affected. Seeing how all males that carried the disease were affected at some point the disease must lay dormant in female carriers but not males. This means the original father cannot be a carrier of the disease. Hope this helps!

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Predict phenotypes associated with nondisjunction of sex chromosomes.
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Answer: The new daughter cells will have an abnormal amount of genetic material. That is called aneuploidy and it is the presence of an abnormal number of chromosomes. Different clinical conditions are the result of this nondisjunction.

Explanation:

Normal cells are diploids, that means they have two copies of each gene, one of each chromosome. So normal cells have two homologous chromosomes, one from each parent.

During anaphase of cell division, each pair of chromosomes is separated  by the mitotic spindle. The separated chromosomes are then pulled by the spindle to opposite poles of the cell, and eventually will end up in the new daughter cells.

Nondisjunction is the failure of homologous chromosomes to separate properly during cell division, so it is the miss segregation of them. The new daughter cells will have an abnormal amount of genetic material. <u>Different clinical conditions are the result of this nondisjunction.</u>

Sex chromosomes participates in sex determination of an individual. Females have two X chromosomes (XX), while males have one X and one Y chromosome (XY) So nondisjunction of sex chromosomes could be:

  • XX: one cell with no chromosome and the other cell with two X chromosomes.
  • XY: one cell with no chromosomes and the other cell with XY chromosomes.

According to which gametes are fused during fertilization, different phenotypes can be given. For example, if a gamete with one chromosome fuses with another gamete with two chromosomes, the result will be an individual with three chromosomes (it could be XXY, or XXX) called trisomy.

Triple X syndrome is characterized by an extra X chromosome in females. Those affected are often taller than average, but most females have a normal sexual development. Klinefelter syndrome is known XXY individuals, and it causes infertility in males, breast growth, less body hair and weaker muscles.

And if a gamete with no chromosome fuses also with another gamete with no chromosome, the result is a nullisomy. But due to the lack of genetic material, the nullisomic gametes are rendered unviable for fertilization.

And if a gamete with no chromosome fuses with another gamete with one chromosome (normal) the result is a monosomy, the presence of only one chromosome from a pair. The result can be an individual who is X or Y. People with Turner syndrome have one X chromosome and it is the only monosomy that is seen in humans because other cases monosomy are lethal.

Any of those examples is called aneuploidy and it is the presence of an abnormal number of chromosomes.

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