Exam 1 Bio Study Guide Flashcards
(38 cards)
In rabbits, there is a gene that controls ear length, with a dominant allele “T” for long ears and a recessive allele “t” for short ears. At another gene locus, there are alleles “B” for black and “b” for white coats. Neither the B or b allele is dominant and Bb produces a gray coat. These two alleles pairs assort independently. If a gray rabbit that is heterozygous at the gene locus controlling ear length is mated with a white rabbit that is also heterozygous at the gene locus controlling ear length, what is proportion of the long-eared offspring will be homozygous for the long-eared trait?
1/3
Two parents each have blood type AB, and their first child has blood type AB. What is the probability that their second child will have blood type AB?
50%
Consider the cross AaBbCcddEe x AABBccDDEe. If these 5 allele pairs assort independently, then the probability that any individual offspring will have the genotype AABBccDdEe is 1 out of___.
16
Different phenotypes produced for the same genotype due to environmental variation is called ___
Phenotypic Plasticity
A genetic __ indicated the distances between gene loci measured in terms of frequency of recombination.
map
Traits that are controlled by genes located on the X chromosome are said to be___.
sex-linked
What is the relationship between recombination frequency and the actual physical distance on a chromosome?
As physical distance increases, the recombination frequency first increases in a linear fashion, but eventually reaches a maximum of 0.5 or 50%
Pedigrees are useful to genderists because they can help determine
a. The mode of inheritance for a particular trait
b. The genotype of a particular individual
c. The probability that future offspring will inherit a particular trait
d. Whether a particular trait is dominant or recessive
Messenger RNA molecules contain information that is used to synthesize
Polypeptides
To begin transcription, RNA polymerase must bond to a segment of DNA called the ___.
Promoter
The strand of DNA that is not transcribed is called the ___ strand.
Coding
A codon is composed of how many bases?
3
In eukaryotic cells, transcription occurs
Inside the nucleus
If the sequence of bases in the template strand of a DNA molecules is 3’ ATCGCTCC 5’, what is the sequence of bases in the RNA that is transcribed from this molecule?
5’ UAGCGAGG 3’
What is the fist step during transcription initiation in prokaryotes?
RNA polymerase binds to the promoter
You are helping to decode some genome seqnece. Unfortunately the sequencing compony forgot to tell you which is the 5’ and 3’ ends of the double-stranded DNA sequence below. However, know that the sequence codes for Met-Leu-Trp…
Strand #1 ACAATGAGGCCAGAGCATAAT; Strand #2 TGTTACTCCGGTCTCGTATTA
2, right to left
In humans, RNA polymerase begins transcription at a ___ and stops at a___
Promoter, termination sequence
Genes that are very far apart on a long autosome are:
So likely to have crossing over that they appear to assort independently
Which of the following correct about reading genes on a chromosome ( a double stranded DNA molecule)?
One strand is read as template for each gene, with the strand serving as template differing for various genes
The START codon is:
The first AUG after the +1 transcription initiation site
In leopards, dark spots (D) are dominant to light spots (d). A separate epistatic gene controls the presence of spots. Lack of spots (n) is recessive to the presence of spots (N). P1 has offspring with a mate that has dark spots (P2). The offspring include animals with dark spots, light spots, and no spots, what are the genotypes of the parents?
P1: Nndd P2: NnDd
Cystic fibrosis in humans is caused by mutations in a single gene and is inherited as an autosomal (non-sex chromosome) recessive trait. A normal couple has two children. The first child has cystic fibrosis, and the second child is unaffected. Given that you know the second child’s phenotype, what is the probability that the second child is a carrier (heterozygous) for the mutation that causes the disease?
2/3
In the germline cell below, there are two pairs of chromosomes on which are shown the locations of tw different genes. F and f represent two different alleles (versions or variants) of one gene, and Q and q represent two different alleles of another egen. If this cell divides normally to produce sperm, what are the possible sperm genotypes.
FQ, fq, Fq, fQ
Deviations from expected rations (9:3:3:1, for example) found in Mendelian genetics caused by epistasis or complementation are proof that ___?
The gene products of different genes can both affect a phenotype