The pedigree chart represents three generations. Red family members have a disease that is caused by an autosomal dominant gene. Consider the chart. The father in Generation I must have what genotype? D represents the allele for the disease; d the allele for normal. A) DD B) Dd C) XDYD D) XDYd

the father have the genotype of Dd.

Explanation:

As the desies is autosomal dominant so their is no involvement of sex chromosome and the presence of any dominant allel on an autosome will cause the desies to occur in the individual. As their are two types of chromosome in individual the sex chromosomes and the autosomes.as the desies is dominant so their will be no skip generation and no carier in the pedigree with the presence of one allel will result in apperance of the desise.The desies is autosomal so the male and female individuals are equally effected.

gametes or germ cells are haploid cells (example: sperm and ova) containing only one set (or n) number of chromosomes and autosomal or somatic cells are diploid cells containing 2n number of chromosomes.

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.