all red Flashcards
(28 cards)
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.
c) participation in
construction of a nucleolus; d) participation in construction of ribosomes.
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.
b)
formation of lysosomes; c) formation of inclusions; d) excretory and secretory
functions.
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-formation of the mitotic spindle;
c) uniform
distribution of chromosomes in a mitosis and a meiosis;
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.
b) provide satiation of chromosomes; c)
preserve a chromosome as discrete unit; d) interfere with bond of chromosomes
or their fragments among themselves.
Kinds of mitosis:
mitosis, meiosis; b) endomitosis, polyteny; c) amitosis.
mitosis, meiosis; b) endomitosis, polyteny;
What is transported to cell poles in an anaphase of a mitosis?
chromatids
The periods of a spermatogenesis:
a)
reproduction, growth, formation; b) reproduction, formation, maturation;
c) growth, maturation, formation; d) reproduction, growth, maturation,
formation.
d) reproduction, growth, maturation,
formation.
The periods of an ovogenesis:
a-reproduction, growth, maturation; b) reproduction, formation, maturation;
c) growth, maturation, formation; d) reproduction, growth, formation,
maturation.
a-reproduction, growth, maturation;
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.
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.
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.
c)
has a mosaic constitution, operon includes one structural gene.
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.
d) contains the information of polypeptide
structure.
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.
d) contains the information on frame of protein-repressor.
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.
c) increase or decrease the speed of
biochemical reactions;
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.
b) passes or
quenches transit m-RNA-polymerase to structural genes;
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.
c)
disorders of secondary sexual attributes formation.
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)
disorders of secondary sex attributes formation;
c) sclerotic disorders in semeniferous tubules.
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.
b) pigment retinitis, pigmentosum
xeroderma;
c) hemorrhage diathesis, total color-blindness;
The illnesses with completely sex-linked inheritance:
hemophilia C; b) hemophilia A and B; c) daltonism, Dushene muscular
dystrophia; d) hemorrhagic diathesis.
b) hemophilia A and B; c) daltonism, Dushene muscular
dystrophia;
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.
b) genes are located in same chromosome and are inherited
together;
Kinds of cytoplasmic inheritance:
a) cytoplasmic inheritance itself; b) mitochondrial; c)
cytoplasm predetermination; d) pseudo-cytoplasmic inheritance.
a) cytoplasmic inheritance itself; b c)
cytoplasm predetermination; d) pseudo-cytoplasmic inheritance.
Types of local changes in gene mutations:
a)changing, translocation of nucleotides pair; b) insert or deletion of nucleotides
pair; c) deficiency, deletions.
a)changing, translocation of nucleotides pair; b) insert or deletion of nucleotides
pair;
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.
b) parts of polypeptide are synthesized;
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)destruction of telomere on the ends of chromosomes;
Examples of semilethal mutations of human:
a)daltonism; b) Dawn syndrome; c) trisomy on X-chromosome; d) hemophilia;
e) muscular dystrophia Duchenne.
b) Dawn syndrome;
d) hemophilia;
e) muscular dystrophia Duchenne.