LIFE SCIENCE

OBJECTIVE LIFE SCIENCE

MOLECULAR BIOLOGY

Question [CLICK ON ANY CHOICE TO KNOW THE RIGHT ANSWER]
Sickle Cell AnemiaSequence for Normal HemoglobinDNA Sequence ATGGTG CAC CTG ACT CCT GAG GAG AAG TCT GCC GTT ACTAmino Acid Seq.STARTValHisLeuThrProGluGluLysSerAlaValThe Sequence for Sickle Cell HemoglobinDNA Sequence ATGGTG CAC CTG ACT CCT GTG GAG AAG TCT GCC GTT ACTAmino Acid Seq.STARTValHisLeuThrProValGluLysSerAlaValWhat mRNA would be transcribed from the normal hemoglobin DNA?
A
TAC CAC GTG GAC TGA GGA CAC CTC TTC AGA CGG CAA TGA
B
UAC CAC GUC GAC UGA GGA CUC CUC UUC AGA CGG CAA UGA
C
UAC CAC GUG GAC UGA GGA CAC CUC UUC AGA CGG CAA UGA
D
TAC CAC GTC GAC TGA GGA CTC CUC TTC AGA CGG CAA TGA
Explanation: 

Detailed explanation-1: -Normal hemoglobin contains the amino acid glutamate at position 6 in the primary sequence. In individuals with sickle-cell disease, this glutamate is replaced with the amino acid valine.

Detailed explanation-2: -Genetic studies have shown that the base sequence in normal hemoglobin (HbA) and sickle cell hemoglobin (HbS) differs at only one position (a change from an A to a T). This change to one codon results in a single amino acid change in the hemoglobin.

Detailed explanation-3: -Sickle cell anaemia gets its name from the abnormal shape of the erythrocytes, which resemble that of an old farming tool, the sickle (Figure 13). This shape is due to a single nucleotide substitution (A to T) that converts a glutamic acid codon (GAG) into a valine codon (GUG) in the beta chains of Hb.

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