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A Mutagenesis Screen Performed on Mice Identified a Gene with an Important

Question 25

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A mutagenesis screen performed on mice identified a gene with an important function in B cells. Analysis of B cells from the spleens of these mutant mice showed the results shown in Figure. However, when the C δ\delta coding sequences were determined, no mutations in these DNA sequences were found. To study this further, genetic crosses were set-up with another mouse strain carrying an allelic variant of the immunoglobulin heavy chain locus. The original mutant mouse strain (strain A) carries IgMa and IgDa alleles of these heavy chain genes. The second mouse strain (strain B) carries the IgMb and IgDb alleles of the heavy chain genes. These two parental strains were crossed together, generating progeny that were all heterozygous for IgM and IgD alleles B were obtained.  A mutagenesis screen performed on mice identified a gene with an important function in B cells. Analysis of B cells from the spleens of these mutant mice showed the results shown in Figure. However, when the C \delta  coding sequences were determined, no mutations in these DNA sequences were found. To study this further, genetic crosses were set-up with another mouse strain carrying an allelic variant of the immunoglobulin heavy chain locus. The original mutant mouse strain (strain A)  carries IgM<sup>a</sup> and IgD<sup>a</sup> alleles of these heavy chain genes. The second mouse strain (strain B)  carries the IgM<sup>b</sup> and IgD<sup>b</sup> alleles of the heavy chain genes. These two parental strains were crossed together, generating progeny that were all heterozygous for IgM and IgD alleles B were obtained.        Based on these data, the mutation in the original mutant mouse strain most likely inactivates: A)  The gene for a transcription factor required for IgD gene transcription B)  A regulatory region in the immunoglobulin heavy chain gene locus required for IgD gene transcription C)  The gene for a factor required for alternative mRNA splicing of the immunoglobulin heavy chain primary mRNA transcript D)  The gene encoding the RAG-1 or RAG-2 recombinase E)  The gene for a factor that is required for IgD surface expression
 A mutagenesis screen performed on mice identified a gene with an important function in B cells. Analysis of B cells from the spleens of these mutant mice showed the results shown in Figure. However, when the C \delta  coding sequences were determined, no mutations in these DNA sequences were found. To study this further, genetic crosses were set-up with another mouse strain carrying an allelic variant of the immunoglobulin heavy chain locus. The original mutant mouse strain (strain A)  carries IgM<sup>a</sup> and IgD<sup>a</sup> alleles of these heavy chain genes. The second mouse strain (strain B)  carries the IgM<sup>b</sup> and IgD<sup>b</sup> alleles of the heavy chain genes. These two parental strains were crossed together, generating progeny that were all heterozygous for IgM and IgD alleles B were obtained.        Based on these data, the mutation in the original mutant mouse strain most likely inactivates: A)  The gene for a transcription factor required for IgD gene transcription B)  A regulatory region in the immunoglobulin heavy chain gene locus required for IgD gene transcription C)  The gene for a factor required for alternative mRNA splicing of the immunoglobulin heavy chain primary mRNA transcript D)  The gene encoding the RAG-1 or RAG-2 recombinase E)  The gene for a factor that is required for IgD surface expression
Based on these data, the mutation in the original mutant mouse strain most likely inactivates:


A) The gene for a transcription factor required for IgD gene transcription
B) A regulatory region in the immunoglobulin heavy chain gene locus required for IgD gene transcription
C) The gene for a factor required for alternative mRNA splicing of the immunoglobulin heavy chain primary mRNA transcript
D) The gene encoding the RAG-1 or RAG-2 recombinase
E) The gene for a factor that is required for IgD surface expression

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