Chapter 3 Flashcards

(39 cards)

1
Q

Interchange of genetic material between homologous chromosomes during synapse and meiosis

A

crossover

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2
Q

a disease associated with formation of cell-mediated or humoral immunity against the subjects own cells or tissue components

A

autoimmune disease

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3
Q

the inactivated X chromosome that is applied to the nuclear membrane in the female. Sex Chromatin body.

A

barr body

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4
Q

the genes of histocompatibility complex and the antigens that they determine on the surface of cells

A

HLA system

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5
Q

the structure that joins each pair of chromatids formed by chromosome duplication

A

centromere

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6
Q

the gene present on the X chromosome

A

sex-linked gene

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7
Q

germ cells in a late stage of sperm development just before complete maturation to form mature sperm

A

spermatids

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8
Q

cells lining the ovarian follicles

A

granulosa cells

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9
Q

same as recombinant DNA technology

A

gene splicing, genetic engineering

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10
Q

structure extruded during the meiosis of the oocyte. Contains discarded chromosomes and a small amount of cytoplasm

A

polar body

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11
Q

the general term referring to either ovary or the testis

A

gonad

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12
Q

a noncoding part of a chromosomal DNA chain

A

intron

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13
Q

unique histocompatability antigens (self-antigens) on the surface cells. Also called major histocompatibility complex (MHC) antigens

A

human leukocyte antigens

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14
Q

the type of cell division of most cells in which chromosomes are duplicated in the daughter cells and are identical with those in the parent cell. the characteristic cell division found in all cells in the body except for gametes.

A

mitosis

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15
Q

a systemic disease primarily affecting the synovium with major manifestations in the small joints

A

rhumatoid arthritis

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16
Q

methods for combining gene from one organism, with genes of another organism

A

recombinant DNA technology

17
Q

the position of a gene on a chromosome. different forms (alleles) of the same gene are always found at the same locus on a chromosome

18
Q

pairing of homologous chromosomes in meiosis

19
Q

an arrangement of chromosomes from a single cell arrangement in pairs in descending order according to size of the chromosomes and the positions of the centromeres

20
Q

reproductive cells, eggs, and sperm each containng 23 chromosomes which unite during fertilization to form a zygote containing 46 chromosomes

21
Q

the total of all the genes contained in a cell’s chromosomes.

22
Q

a term applied to genes located on the X chromosome in the male

23
Q

a gene that expresses a trait on the heterozygous state

A

dominant gene

24
Q

a small circular DNA molecule separate from the main bacterial chromosome.

25
a group of genes on chromosome 6 that determine the antigens on the surface cells
major histocompatability complex
26
a chromosome other than a sex chromosome
autosome
27
one of several related genes that may occupy the same locus on a homologous chromosome
allele
28
the development of mature eggs and sperm from precursor cells
gametogenesis
29
a protein or enzyme specified (coded) by a gene
gene prodcut
30
a special type of cell division occurring in gametes (ova and sperm) in which the number of chromosomes is reduced by one-half in the ovum and sperm
meiosis
31
the part of a chromosomal DNA chain that codes for a specific protein or enzyme
exon
32
having two different alleles at given gene loci on the homologous pair of chromosome
heterozygous
33
one of two newly formed chromosomes held together by the centromere
chromatid
34
the X and Y chromosomes that determine genetic sex
sex chromosomes
35
a soluble growth promoting substance produced by cells that hesitates to receptors on the cell membrane of other cells, which activates the receptors and initiates events leading to growth or division of the target cells
growth factor
36
a cell resulting from division of a single call
daughter cell
37
a set of HLA genes on one chromosome that is transmitted as a set
haplotype
38
a matched pair of chromosome one derived from each parent
homozygous chromosomes
39
a gene that expresses a trait only when present in the homozygous state
recessive gene