Chapter 1 Cell Function Flashcards

1
Q
Contains chromatin and nucleolus
At least one per cell
Control center
Genetic code
Nucleoli
A

Nucleus

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2
Q

Place for cell work
Contains water, electrolytes, suspended proteins, neutral fats, and glycogen
Contains the organelles

A

Cytoplasm

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3
Q

Site for protein synthesis
Small particles of nucleoproteins
May be attached to ER or free

A

Ribosomes

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4
Q

Matrix of paired membranes and vesicles
Tubular communication system
place where metabolic activity occurs

A

Endoplasmic reticulum

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5
Q

Produce proteins for membranes and lysosomal enzymes

A

Rough ER

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6
Q

Lipid, lipoprotein, and steroid synthesis; regulation of intracellular Ca, metabolism, and detoxification of hormones and drugs

A

Smooth ER

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7
Q

Site for carb production

A

Golgi apparatus

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8
Q

Break down cell products and foreign bodies to be used again, require acidic environment

A

Lysosomes

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9
Q

Control free radicals

A

Peroxisomes

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10
Q

Power plants, aerobic metabolism-atp
Number in a given cell varies depending on the cell’s energy need
Contains own DNA and ribosomes

A

Mitochondria

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11
Q

Threadlike structure

A

Microfilament

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12
Q
Semipermeable
Contains receptors
Involved in electrical conduction
Regulates cell growth and proliferation
Lipid belayer 
Proteins
A

Cell membrane

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13
Q

Open and close ion channels
Activated G-protein-linked signals
Activate enzyme-linked cell function

A

Membrane receptors

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14
Q

Disorder of connective tissue
Mutation on chromosome 15 (FBN1)
Combines with other fibrillins and gives rise to micro fibrils
Mutation leads to reduced elasticity and excess growth factor release
Affects eyes, skeleton, and cardiovascular system

A

Marfan’s Syndrome

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15
Q

Neurogenic tumors
2 forms: type 1 defect on chromosome 17, subcutaneous lesions, cafe’-au-lait spots, freckles, scoliosis, erosive bone defects, and nervous system tumors
Type 2- defect on chromosome 22; tumors of the acoustic nerve

A

Neurofibromatosis

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16
Q

Mutation on chromosome 12 leads to an error in converting phenylalanine to tyrosine
Appears normal at birth then fails to meet milestones
Progressive neurological decline
Can lead to severe intellectual disability

A

PKU

17
Q

Progressive disorder due to mutation of hexosaminidase A
Most are of Jewish decent
3 forms: infantile, juvenile, adult

A

Tay-sachs

18
Q

Associated with single trinucleotide gene sequence on the X chromosome, which is repeated >200 times
Plays a role in synapse development

A

X-linked

19
Q

Improper formation of soft tissue of mouth and lips

A

Cleft lip and palate

20
Q

Risk increases with maternal age

Caused from no disjunction during meiosis

A

Trisomy 21 (Down’s syndrome)

21
Q

Deletion of all or part of an X-occurs spontaneously
Specific gene associated is unknown
No Y chromosome

A

Monosomy X (turner’s syndrome)

22
Q

One of more extra X chromosomes with the presence of the Y
Male appearance
Tx: testosterone

A

Trisomy x