Chapter 6 Flashcards
What genetic process is likely responsible for the occurrence of asthma in only one of a pair of identical twins?
a. Epigenetic modifications
b. Genomic imprinting
c. Transgenerational inheritance
d. Methylation
a. Epigenetic modifications
Prader-Willi syndrome causes a chromosomal defect that is:
a. Initiated by postnatal exposure to a virus
b. Inherited from the father
c. Related to maternal alcohol abuse
d. Transferred from mother to child
b. Inherited from the father
A malfunction in DNA methylation can lead to:
a. Hypothyroidism
b. Blindness
c. Cancer
d. Diabetes mellitus
c. Cancer
Which statement is true regarding the embryonic development of stem cells?
a. They are already differentiated.
b. They are referred to as housekeeping genes.
c. They already demonstrate DNA sequencing.
d. They are said to be pluripotent.
d. They are said to be pluripotent.
When microRNA (miRNA) are methylated their messenger RNA (mRNA) targets are over-expressed, the resulting effect on existing cancer would be:
a. Cell death
b. Metastasis
c. Remission
d. Relapse
b. Metastasis
The difference between DNA sequence mutations and epigenetic modifications is:
a. DNA sequence mutations can be directly altered.
b. Leukemia is a result of only DNA sequence mutation.
c. Epigenetic modifications can be reversed.
d. No known drug therapies are available for epigenetic modifications.
c. Epigenetic modifications can be reversed.
Which term refers to the silenced gene of a gene pair?
a. Activated
b. Altered
c. Mutated
d. Imprinted
d. Imprinted
The shape of the face of a child diagnosed with Russell-Silver syndrome is likely to be:
a. Round
b. Square
c. Triangular
d. Elongated
c. Triangular
Genes responsible for the maintenance of all cells are referred to as:
a. Universal
b. Managerial
c. Housekeeping
d. Executive
c. Housekeeping
What is the belief regarding twins who adopt dramatically different lifestyles?
a. They may experience very different aging processes.
b. They will retain very similar methylation patterns.
c. They will experience identical phenotypes throughout their lifespans.
d. They may never demonstrate similar DNA sequences of their somatic cells.
a. They may experience very different aging processes.
Hypomethylation and the resulting effect on oncogenes result in a(an):
a. Decrease in the activity of of the oncogene, thus suppressing cancer development
b.Deactivation of MLH1 to halt DNA repair
c. Increase in tumor progression from benign to malignant
d. Over-expression of microRNA, resulting in tumorigenesis
c. Increase in tumor progression from benign to malignant
When a chromosome lacking 4 Mb is inherited from the mother, the child is at risk for developing which syndrome?
a. Prader-Willi
b. Angelman
c. Beckwith-Wiedemann
d. Russell-Silver
b. Angelman
A child’s diagnosis of Beckwith-Wiedemann syndrome is supported by the presence of:
(Select all that apply.)
a. An omphalocele
b. Neonatal hypoglycemia
c. Creased earlobes
d. Low birth weight
e. A large tongue
a. An omphalocele
b. Neonatal hypoglycemia
c. Creased earlobes
e. A large tongue
A diagnosis of Angelman syndrome in a child is supported by which assessment findings?
(Select all that apply.)
a. Small feet and hands
b. Profound cognitive dysfunction
c. Obesity
d. Ataxic gait
e. History of seizures
b. Profound cognitive dysfunction
d. Ataxic gait
e. History of seizures