all red Flashcards

(28 cards)

1
Q

Role of r-RNA in life activity of a cell:
a)
participation in a transcription in a biosynthesis of proteins; b)
participation in translation in a biosynthesis of proteins; c) participation in
construction of a nucleolus; d) participation in construction of ribosomes.

A

c) participation in
construction of a nucleolus; d) participation in construction of ribosomes.

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1
Q

Role of Golgi complex in a cell:
a)
participates in uniform movement of chromosomes to cell poles; b)
formation of lysosomes; c) formation of inclusions; d) excretory and secretory
functions.

A

b)
formation of lysosomes; c) formation of inclusions; d) excretory and secretory
functions.

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2
Q

Role of centrioles in a cell:
a-formation of the mitotic spindle; b) formation of lysosomes; c) uniform
distribution of chromosomes in a mitosis and a meiosis; d) excretory function.

A

a-formation of the mitotic spindle;
c) uniform
distribution of chromosomes in a mitosis and a meiosis;

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3
Q

Role of telomeres in chromosomes:
a)
participate in division of a cell; b) provide satiation of chromosomes; c)
preserve a chromosome as discrete unit; d) interfere with bond of chromosomes
or their fragments among themselves.

A

b) provide satiation of chromosomes; c)
preserve a chromosome as discrete unit; d) interfere with bond of chromosomes
or their fragments among themselves.

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4
Q

Kinds of mitosis:
mitosis, meiosis; b) endomitosis, polyteny; c) amitosis.

A

mitosis, meiosis; b) endomitosis, polyteny;

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5
Q

What is transported to cell poles in an anaphase of a mitosis?

A

chromatids

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6
Q

The periods of a spermatogenesis:
a)
reproduction, growth, formation; b) reproduction, formation, maturation;
c) growth, maturation, formation; d) reproduction, growth, maturation,
formation.

A

d) reproduction, growth, maturation,
formation.

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7
Q

The periods of an ovogenesis:
a-reproduction, growth, maturation; b) reproduction, formation, maturation;
c) growth, maturation, formation; d) reproduction, growth, formation,
maturation.

A

a-reproduction, growth, maturation;

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8
Q

Features of prokaryote gene expression:
a)
group repression of genome genes is possible; b) group repression of
chromosome genes, genome and regulation of expression by steroid hormones
are not possible; c) the genes monitoring one biochemical reaction locate in one
place.

A

b) group repression of
chromosome genes, genome and regulation of expression by steroid hormones
are not possible; c) the genes monitoring one biochemical reaction locate in one
place.

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9
Q

Features of eukaryote gene construction:
has no mosaic constitution; b) operon consists some structural genes; c)
has a mosaic constitution, operon includes one structural gene.

A

c)
has a mosaic constitution, operon includes one structural gene.

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10
Q

Function of structural genes:
contain the information on synthesis t-RNA and г-RNA; b) increase or
decrease the speed of biochemical reactions; c) contain the information on
structure of protein-repressor; d) contains the information of polypeptide
structure.

A

d) contains the information of polypeptide
structure.

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11
Q

Function of a gene-regulator:
a)
increase or decrease the speed of biochemical reactions; b) contains the
information on synthesis t-RNA, r-RNA; c) contains the information of enzyme
structure; d) contains the information on frame of protein-repressor.

A

d) contains the information on frame of protein-repressor.

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12
Q

Function of modifiers genes:
find necessary m-RNA-polymerase; b) passes or quenches transit of the
RNA - polymerase to structural genes; c) increase or decrease the speed of
biochemical reactions; d) suppress transcription.

A

c) increase or decrease the speed of
biochemical reactions;

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13
Q

Function of the gene-operator:
contains the information on structure of protein-repressor; b) passes or
quenches transit m-RNA-polymerase to structural genes; c) finds necessary
m-RNA- polymerase; d) cap-proteins binding.

A

b) passes or
quenches transit m-RNA-polymerase to structural genes;

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14
Q

Influence on human sex formation of change of autosomes and sex
chromosome ratio at caryotype XXX: 44A (additional X-chromosome in
woman):
a)
underdevelopment of uterus, ovaries; b) disorders of a menstrual cycle; c)
disorders of secondary sexual attributes formation.

A

c)
disorders of secondary sexual attributes formation.

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15
Q

Influence on human sex formation of change of autosomes and sex
chromosome ratio at caryotype XXY: 44A (Kleinefelter syndrome):
a)
disorders of secondary sex attributes formation; b) underdevelopment of
generative organs; c) sclerotic disorders in semeniferous tubules.

A

a)
disorders of secondary sex attributes formation;
c) sclerotic disorders in semeniferous tubules.

16
Q

The illnesses with partially sex-linked illnesses inheritance:
a)
Duschene muscular dystrophy; b) pigment retinitis, pigmentosum
xeroderma;
c) hemorrhage diathesis, total color-blindness; d) syndactylia.

A

b) pigment retinitis, pigmentosum
xeroderma;
c) hemorrhage diathesis, total color-blindness;

17
Q

The illnesses with completely sex-linked inheritance:
hemophilia C; b) hemophilia A and B; c) daltonism, Dushene muscular
dystrophia; d) hemorrhagic diathesis.

A

b) hemophilia A and B; c) daltonism, Dushene muscular
dystrophia;

18
Q

Complete linkage of genes:
a)
genes are located in different chromosomes and are free combined with
each other;
b) genes are located in same chromosome and are inherited
together; c) genes are located in same chromosome; the part of them is inherited
together, and the part is combined by a crossing-over.

A

b) genes are located in same chromosome and are inherited
together;

19
Q

Kinds of cytoplasmic inheritance:
a) cytoplasmic inheritance itself; b) mitochondrial; c)
cytoplasm predetermination; d) pseudo-cytoplasmic inheritance.

A

a) cytoplasmic inheritance itself; b c)
cytoplasm predetermination; d) pseudo-cytoplasmic inheritance.

20
Q

Types of local changes in gene mutations:
a)changing, translocation of nucleotides pair; b) insert or deletion of nucleotides
pair; c) deficiency, deletions.

A

a)changing, translocation of nucleotides pair; b) insert or deletion of nucleotides
pair;

21
Q

Consequences of a nonsense mutation:
a)new protein is synthesized; b) parts of polypeptide are synthesized; c) there is
a changing of several amino acids in a polypeptide.

A

b) parts of polypeptide are synthesized;

22
Q

Mechanisms of appearance of chromosome aberrations:
a)destruction of telomere on the ends of chromosomes; b) breaking of process
of a crossingover; c) breaking of divergence of chromosomes at mitosis and
meiosis.

A

a)destruction of telomere on the ends of chromosomes;

23
Q

Examples of semilethal mutations of human:
a)daltonism; b) Dawn syndrome; c) trisomy on X-chromosome; d) hemophilia;
e) muscular dystrophia Duchenne.

A

b) Dawn syndrome;
d) hemophilia;
e) muscular dystrophia Duchenne.

24
Dermatogliphical parameters of Klinefelter’s syndrome: a)low papillary lines set, big distance between lines; b) predominance of ulnar loops; c) predominance of arches; d) a four-digital sulcus; e) angle atd = 40° - 42°.
a)low papillary lines set, big distance between lines; c) predominance of arches; e) angle atd = 40° - 42°
25
Opportunities of a cytogenetic method: a)allows to establish hereditary diseases linked to change of chromosomes number and structure, a translocation; b) to define phylum and variant of inheritance; c) to define hereditary diseases of a metabolism
a)allows to establish hereditary diseases linked to change of chromosomes number and structure, a translocation;
26
Entoderm derivatives: a) epithelium of a foregut and hindgut; b) epithelium of an middle gut; c) epithelium of the respiratory system; d) digestive glands.
b) epithelium of an middle gut; c) epithelium of the respiratory system; d) digestive glands.
27
Hypothesis of acceleration: a) enough noutrishment; b) influence of earth magnetic field; c) high action of electromagnet rays by TV and radio; d) appearance of heterosis.
a) enough noutrishment; b) influence of earth magnetic field; c) high action of electromagnet rays by TV and radio; d) appearance of heterosis.