Chromosome Structure: Questions Answered

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In summary: In this scenario, the two genes would be read in opposite directions on opposite strands of DNA. In summary, a chromosome is made up of two sister chromatids during mitosis, which are identical except for any replication errors. Chromatin refers to the complex of DNA and proteins, while chromatids are the linear DNA molecules that make up our genome. The centromere is the sequence of DNA that connects to microtubules during mitosis, and the kinetochore is the protein complex that forms at the centromere during mitosis. While most coding sequences have only one gene on one strand of DNA, there are some viruses that have overlapping genes on opposite strands.
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zmike
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I am in intro to genetics class and I am getting really confused with the terminology:

-Is a chromosome made up of 2 sister chromatids?
-are the 2 sister chromatids identiical?
-what's the difference between chromatins and chromatids? and between the kinetochore and centromere?

-gene structure: I saw a diagram showing this for a double helix DNA strand where gene X and gene y start and end at the same location on opposite strands

5' --------GENE X--------3'
3' --------GENE Y--------5'

If the 2 strands are complementary how can 2 genes be at the same location? since it's read 5' to 3' by the RNA transcriptase?

Thank you so very much!
 
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zmike said:
-Is a chromosome made up of 2 sister chromatids?

A chromosome, during mitosis, is made up of two sister chromatids. However, the term chromosome can also sometimes be used to refer to an individual chromatid (for example, during most of the cell cycle where our chromosomes are uncompacted).

-are the 2 sister chromatids identiical?
Yes (excluding any errors that occurred during replication).

-what's the difference between chromatins and chromatids? and between the kinetochore and centromere?

Is the general term used to describe the complex between genomic DNA and the proteins coating it (most notably the histone proteins). Chromatids refer to one of the linear DNA molecules that make up our genome.

The centromere is the sequence(s) of DNA that connect to microtubules and motor proteins during mitosis. The kinetochore is the term that refers to the complex of proteins and DNA that forms at the centromere during mitosis. The difference is subtle, but here is an example of how they are different. The centromere is always present on the chromosomes (even in the absence of the proteins that connect to it during mitosis), but the kinetochore forms only when the correct proteins assemble on the centromere during mitosis.

-gene structure: I saw a diagram showing this for a double helix DNA strand where gene X and gene y start and end at the same location on opposite strands

5' --------GENE X--------3'
3' --------GENE Y--------5'

If the 2 strands are complementary how can 2 genes be at the same location? since it's read 5' to 3' by the RNA transcriptase?

Most coding sequences in our DNA would have only one gene on one strand at that location. At the location of a gene, one DNA strand that acts as a template for the synthesis of mRNA and the non-template strand is not used for anything. However, some viruses, whose genomes must be much more compact than ours, do have overlapping genes where the non-template strand contains the information for a different protein.
 

FAQ: Chromosome Structure: Questions Answered

1. What is a chromosome?

A chromosome is a thread-like structure found in the nucleus of a cell that contains genetic information in the form of DNA.

2. How many chromosomes do humans have?

Humans have 23 pairs of chromosomes, for a total of 46 chromosomes.

3. What is the structure of a chromosome?

A chromosome has a characteristic X-shaped structure, with two arms joined by a central region called the centromere. The arms are made up of tightly coiled DNA and proteins called chromatin.

4. How are chromosomes organized in the nucleus?

Chromosomes are organized in the nucleus by being tightly wound and folded into a compact structure. They are also attached to structures called the nuclear lamina, which helps maintain their position in the nucleus.

5. How do changes in chromosome structure affect an organism?

Changes in chromosome structure, such as deletions, duplications, or inversions, can result in genetic disorders or developmental abnormalities. These changes can alter the expression of genes, leading to a wide range of effects on the organism.

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