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So I am new to biology and I have been reading, and searching the web, but I couldn't understand the whole framework of a cell. So as I understood:

A DNA, is a double chain of Nucleotides (A,T,G,C and a sugar) and a phosphate residue. Some parts of a DNA code a gene and some do not, exons and introns accordingly. As I understand it these the sequences of exons hold genes and the whole sequence is called genome. Now I read in the book Introduction to Computational Molecular Biology by J. C. Setubal and J. Meidanis. that I cite Each cell of an organism has a few very long DNA molecules. Each such molecule is called a chromosome. So each X shaped thing called a chromosome holds one DNA molecule?

Or is each "hand" of the chromosome one complete double helix of DNA so we have 23 pairs of such chromosomes? or is it that each we 23 pairs Xs?

Shouldn't we have just one uniquely identifiable DNA sequence? I am asking this, because I have also read that each chromosome encodes a different part of one's genome. Does this mean we have several DNA sequences?

This is really bothering me, since I can't figure out the correct structure of a cell.

EDIT:
Now if each chromosome contains a pair of DNA helices. We have 46 chromosomes so overall within the cell there are 92 DNA sequences? All of which are the same? Or are they different? If they are different how do they code for different aspects of one's genome?

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closed as too broad by MattDMo, AliceD, kmm, rg255, James Jun 23 '16 at 7:22

Please edit the question to limit it to a specific problem with enough detail to identify an adequate answer. Avoid asking multiple distinct questions at once. See the How to Ask page for help clarifying this question. If this question can be reworded to fit the rules in the help center, please edit the question.

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Your understanding of DNA is correct. DNA is a heteropolymer of monomers called nucleotides and each nucleotide is made up of a sugar (deoxyribose), phosphate and a "base" (A, T, G, C).

As you already know, DNA is organized as a double helix with the Watson-Crick pairing rules.

A chromosome contains a single DNA double helix. Many organisms have multiple chromosomes which are very different in their DNA sequence. In diploid cells (such as the somatic cells in humans), each chromosome has two copies. The two copies are almost identical and are called "homologous chromosomes". As you know each parent contributes to one of the homologous chromosomes.

During eukaryotic cell division, each chromosome is duplicated. The duplicates (or sister chromatids), are joined at a region which is called the centromere. Centromere is an attachment point for spindle fibres that pull the sister chromatids apart.

Each chromosome has multiple genes. A gene is a region of DNA that is transcribed i.e. it can give rise to an RNA (which can either be a mRNA that in turn codes for proteins or a non-coding RNA). There are other regions of DNA that are not transcribed and these are generally referred to as intergenic regions. In many eukaryotic genes some parts of the transcribed RNAs are removed as a result of splicing. The retained parts are called exons and the removed parts are called introns.

Some organelles like mitochondria and chloroplasts also have a unique genome within themselves. A genome is the entire set of chromosomes including the homologous chromosomes and the organellar chromosomes.

However, when talking about a reference genome, which is just a bioinformatic information and not an actual genome, we just have one sequence for each unique chromosome (for example, in humans, chromosomes 1-22, X-chromosome, Y-chromosome and the mitochondrial DNA). A reference genome is used as a basal set and in a population genomics study, differences from the references are highlighted instead of presenting the entire sequences.

enter image description here Picture source: https://cnx.org/contents/9TxHOD3O@4/The-Nucleus-and-DNA-Replicatio

Note that paired chromosomes (X shape) are found only during replication. Usually the chromosome is like a single thread. Chromatin is the name of the assembly (for e.g., we don't say chromatin-21).


Bottomline: We have 46 chromosomes then it means we technically have 92 DNA sequences. However you should consider the double helix as one entity (or a metamolecule) because the strands always stay together. For more details you should read a book. Genes by Benjamin Lewin and Molecular Biology of the Gene by James Watson et al. are good books on this topic.

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  • $\begingroup$ By saying "Many organisms have multiple chromosomes which are very different in their DNA sequence." You mean that each of my 22 (3) chromosomes has a different DNA helix? Or did you mean that different species have different helices? I'm assuming the former (well obviously the latter is also true) given what you wrote about reference genome, but I am still under the impression that all organism should have just one DNA sequence. I am sorry, my English isn't very good. $\endgroup$ – Vahagn Tumanyan Jun 20 '16 at 13:47
  • $\begingroup$ @VahagnTumanyan Yes each chromosome has a different DNA helix. Different species have different number and composition of chromosomes and within each species the chromosomes will have different sequence. $\endgroup$ – WYSIWYG Jun 20 '16 at 13:51
  • $\begingroup$ I'd suggest adding some images to illustrate this answer - it's the sort of problem some people will understand better with pictures. $\endgroup$ – arboviral Jun 20 '16 at 14:05
  • $\begingroup$ @arboviral Done $\endgroup$ – WYSIWYG Jun 20 '16 at 14:36
  • $\begingroup$ @WYSIWYG and now upvoted! :) $\endgroup$ – arboviral Jun 20 '16 at 15:16

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