Go Deep! Look at the Parent Chromsomes and Key pictured below. Would it be possible for these parents to have a daughter with Hemophilia?

No, the daughter will be a carrier only.

Explanation: Hemophilia is a sex-linked recessive disorder. The recessive gene is carried on the X chromossome. Males have only one X chromossome, while females have 2. So, for a male individual to have hemophilia, it only needs the recessive gene to be on the X chromossome. In a female, the disorder is expressed when both X chromossomes has the recessive gene.

In the Parent Chromossomes picture shown, the father's X chromossome doesn't have the gene for hemophilia and the mother is heterozygous for the trait, i.e., she carries the recessive gene.

A daughter will inherit an X chromossome from the father and an X chromossome from the mother.

In this family, the daughter will inherit the X with dominant gene H for the father and has a possibility of inheriting another dominant gene H or recessive gene h from the mother.

For the daughter to be hemophiliac, she has to inherit 2 recessive genes. Since in either case she won't, she only inherits 1 recessive gene, the daughter will be a carrier for the trait, not have the disease.

transcription is a process in which information is rewritten. it is something our cells must do, in a more specialized and narrowly defined way. in biology, transcription is the process of copying out the dna sequence of a gene in the similar alphabet of rna. it needs to happen in the nucleus because that's where the dna is. dna is always inside the nucleus unless the cell is dividing.

transcription is the first step in gene expression, which involves copying a gene's dna sequence to make an rna molecule. transcription is performed by rna polymerases. it has three stages: initiation, elongation, and termination. rna molecules must be processed after transcription in eukaryotes.

explanation:

long version:

the protein synthesis consists two processes which are, transcription and translation. transcription takes place in the nucleus. it uses dna as a template to make an rna molecule. rna then leaves the nucleus and goes to a ribosome in the cytoplasm, where translation occurs. transcription is the first part of the central dogma of molecular biology: dna → rna. it is the transfer of genetic instructions in dna to messenger rna (mrna). during transcription, a strand of mrna is made that is complementary to a strand of dna.  

these three stages are:

  initiation: in which   is the beginning of transcription.occuring when the enzyme rna polymerase binds to a region of a gene called the promoter. this signals the dna to unwind so the enzyme can ‘‘read’’ the bases in one of the dna strands. the enzyme is now ready to make a strand of mrna with a complementary sequence of bases.

    elongation: in which is the addition of nucleotides to the mrna strand. rna polymerase reads the unwound dna strand and builds the mrna molecule, using complementary base pairs. there is a brief time during this process when the newly formed rna is bound to the unwound dna. during this process, an adenine (a) in the dna binds to an uracil (u) in the rna.

    termination: in which is the ending of transcription, and occurs when rna polymerase crosses a stop (termination) sequence in the gene. the mrna strand is complete, and it detaches from dna.

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