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142 Cards in this Set
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Branch of genetics that deals with chromosomes |
Cytogenetics |
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English chemist, X-ray crystallographer – instrumental in the discovery of DNA like Crick and Watson o used X-ray diffraction to determine the structure of DNA molecules o Her Photo 51 helped scientists learn more about the three-dimensional structure of DNA and enabled scientists to understand DNA´s role in heredity |
Rosalind Franklin |
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physicist, molecular biologist o X-ray crystallography equipment 1954 o Assisted the Watson-Crick discovery/establishment of the chemical structure of DNA |
Maurice Wilkins |
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• Linear end-to-end arrangement of genes and other DNA, sometimes with associated proteins and ribonucleic acid |
Chromosomes |
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tip/end of the chromosomes o made of repetitive sequences of non-coding DNA that protect the chromosome from damage. Each time a cell divides, the ______ become shorter. Eventually, they become so short that the cell can no longer divide o specific DNA–protein structures found at both ends of each chromosome, protect genome from nucleolytic degradation, unnecessary recombination, repair, and interchromosomal fusion. It therefore play a vital role in preserving the information in our genome. |
Telomeres |
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specialized region DNA on each eukaryotic chromosome that acts as a site for the binding of kinetochore proteins |
Centromere |
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less-condensed chromosomal region, thought to contain most of the normally functioning genes o defined as the area of the chromosome which is rich in gene concentration and actively participates in the transcription process o the genetically active region of the chromosome. It contains structural genes that are replicated during G1 and S phase of interphase by allowing polymerases to access the genes |
Euchromatin |
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cytologically dense material that is typically found at centromeres and telomeres. It mostly consists of repetitive DNA sequences and is relatively gene poor. Its most notable property is its ability to silence euchromatic gene expression. |
Heterochromatin |
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Types of chromosomes based on the position of the centromere |
- Metacentric - Submetacentric - Acrocentric - Telocentric |
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same length p and q arms |
Metacentric |
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shorter p arm |
Submetacentric |
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very short p arm |
Acrocentric |
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no p arm |
Telocentric |
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Forms of chromosomes |
- Autosomal (autosomes) - sex |
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• Complete set of chromosomes that are arranged in order size • Each species and sex have different karyotype characteristic (e.g., shape, size, number) |
Karyotype |
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CHROMOSOMES OF DOMESTIC ANIMALS |
- Haploid - Diploid |
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cells contain half of the chromosomes (e.g., reproductive cells) |
Haploid |
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– cells with 2 members of each chromosome pair - (2n, where n=number of chromosome pair in a species) |
Diploid |
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Adult female |
Dam |
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Adult male |
Sire |
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Equine up to 1 yr old |
Foal |
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Equine after 1 year old |
Yearling |
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Swine species as a whole, or any member of it |
Pigs, hog, or swine |
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unweaned young pig, or any immature pig |
Shoat or piglet |
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a pig between birth and weaning. |
Sucker |
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a young pig recently separated from the sow |
Weaning |
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an unusually small and weak piglet, often one in a litter |
Runt |
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male pig of breeding age |
Boar or hog |
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male pig castrated before puberty |
Barrow |
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male pig castrated later in life (an older boar after castration) |
Stag |
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young female not yet mated, or not yet farrowed, or after only one litter (depending on local usage) |
Glit |
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breeding female, or female after first or second litter |
Sow |
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Sheep (_______) and lambs (_______) |
Over 1 year; Less than 1 year |
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fiber that most sheep grow is called _______. The wool from one sheep is called a ________. |
Wool; fleece |
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female lamb |
Ewe |
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young female sheep |
Ewe lamb |
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Process giving birth in sheeps |
Lambing |
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birthing |
Parturition |
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pregnancy |
Gestation |
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male sheep |
Ram |
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is the slang term ram lamb (young male) |
Buck |
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In parts of the United Kingdom, a ram is called a _____ and the mating season is called _______ |
Tup; tupping |
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Shaving of wool in sheep |
Shearing |
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castrated male sheep, less aggressive than rams |
Wethers |
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between 1 and 2 years of age that may or may not have produced offspring. |
Yearling |
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In other countries, a yearling ewe is called a |
hogget, shearling, gimmer, theave, or teg |
HSGTT |
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In goat; ________ (adult male), ________ (young) |
Buck/Billy; bukling |
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In goats: __________ (adult female), ______ (young) |
Doe/Nannys; Doeling |
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Young goats |
Kids |
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Newly Hatched Chicken |
Chick |
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Male chicken that is under a year old |
Cockerel |
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Female that is under a year old |
Pullet |
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A young male or female bird |
Juvenile |
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Male that is a year or older |
Cock |
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Female that is a year or older |
Hen |
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A male chicken (includes cock and cockerel) |
Rooster |
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Refers to small breeds of chicken (AKA Miniature Chicken) |
Bantam |
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Breed of chicken that is raised primarily for egg collection |
Layer breed |
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Breed of chicken that is raised for both eggs and meat |
Dual purpose breed |
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Breed of chicken that is raised primarily for show or exhibition |
Ornamental breed |
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Breed of chicken that is raised for high egg production or meat production |
Production breed |
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Two essential processes in the survival of organisms (especially those reproducing sexually) |
Mitosis and Meiosis |
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True or false: In humans, a somatic cell normally contains 23 pairs of chromosomes (total=46 chromosomes). Twenty-two (22) pairs are autosomes, one pair of sex chromosomes (the X and Y) |
True |
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Nuclear division resulting in _________ |
Gamete formation |
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mature haploid male or female germ cell which is able to unite with another of the opposite sex in sexual reproduction to form a zygote. |
Gamete |
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True or false: Gametes are diploid |
False; they're haploid |
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point of contact, the physical link, between two chromatids belonging to homologous chromosomes |
Chiasma |
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exchange of genetic material can occur between both chromatids, what is called a chromosomal _________ in _________ in Meiosis |
Crossover; Metaphase 1 |
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• for growth and development of an organism • happens in somatic cells |
Mitosis |
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Part of cell cycle of mitosis |
1. Cytokinesis 2. G1 (duplication organelles) 3. S (synthesis/duplication of chromosome) 4. G3 (chromosome duplicated by cell) |
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same type (e.g., chromosome 1 from father and mother and so on) |
Homologous chromosome |
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Is the presence of the Y chromosome enough for the development of a male in mammals? |
NO. There should be full expression of the SRY gene for male to develop |
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Sex inheritance is investigated in early 1900s by __________ |
Thomas Hunt Morgan |
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• Sex chromosome in: X and Y ➢ Females: ➢ Males: |
HOMOGAMETIC (XX) HETEROGAMETIC (XY) |
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• After meiosis ➢ Females: ➢ Males: |
- all gametes contain X chromosome - all gametes contain either X or Y chromosome |
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is important in the expression of doublesex and mab-3 related transcription factor 1 (DMRT 1) gene (present in chromosomes/autosomes) important in the expression of male |
SRY gene |
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Sex chromosomes in avian |
Z and W |
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carries the genes that are essential for the development of female in avian species |
W |
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Female expressed transcript |
FET 1 |
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Avian sex-specific W-linked |
ASW gene |
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In avian species the sex chromosomes for • Females: • Males: |
- HETEROGAMETIC - HOMOGAMETIC |
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Involves a large portion of or multiple genes in the genome |
Chromosome mutations |
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Techniques to assess mutations |
o Microscopy o Genetic or molecular analysis o Combination of techniques |
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Why study chromosome mutations? |
• Provide concepts on how genes interact • Part of genetic manipulation experiments • Give ideas on evolutionary processes • May cause genetic defects |
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Forms of chromosome mutations |
1. Aberration in number 2. Aberration in structure |
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Change in number results in extra or lacking DNA molecules |
Aberration in number |
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Types of aberration in number |
1. Aberrant euploidy 2. Monoploids 3. Aneuploidy - Euploidy - Polyploidy |
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changes in whole chromosome set |
Aberrant euploidy |
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- 1 set of chromosomes - characteristically sterile, gametes are produced by mitosis |
Monoploids |
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changes in parts of chromosome set |
Aneuploidy |
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normal number of chromosomes |
Euploidy |
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– with more than two sets of chromosomes – Common in plants and rare in animals – Increase in the number of chromosomes=origin of new plant species – Often larger and have larger component parts of their diploid relatives |
Polyploidy |
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– individual species that have more than 2 chromosome sets( 3n, 4n, 5n, 6n ) |
Polyploids |
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Is the containment of multiple sets of chromosomes that are derived from the same species |
Autopolyploidy |
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is the containment of multiple sets of chromosomes that are derived from different species. |
Allopolyploidy |
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• with multiple chromosome sets within one species • triploids-characteristically sterile • can arise from nature or can be constructed by a geneticist ➢ crossing a 4n and 2n (2n+n=3n) |
Autopolyploidy |
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• chromosome set made up of two or more chromosome sets from more or less complete from different species; same genus diff species |
Allopolyploidy |
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Forms of aneuploidy |
- Trisomic (2n + 1) - Monosomic (2n - 1) - Nullisomic (2n - 2) - Disomic (2n + 2) |
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only 1 chromosome has 1 extra |
Trisomic (2n + 1) |
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1chromosome is missing |
Monosomic (2n - 1) |
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1 chromosome pair is missing |
Nullisomic (2n - 2) |
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1 c pair has 2 extra chromosomes |
Disomic (2n + 2) |
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Also termed as rearrangement |
Aberration in structure or arrangement |
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Two types of aberration in structure |
1. Unbalanced 2. Balanced |
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Subtypes of unbalanced aberration of structure |
1. Deletions 2. Duplication |
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Subtypes in balanced aberration of structure |
1. Inversion — Pericentric — Paracentric 2. Reciprocal Translocations — Tandem — Centric fusion (Robertsonian translocation) — Centric fission |
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Type of aberration in structure in which there is a change in chromosome’s gene dose |
Unbalanced |
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Type of aberration in structure in which there is a change in gene order |
Balanced |
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— Loss of segment in one chromosome — Assembly of the two segments |
Deletions |
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Only 1 gene is deleted |
Intragenic |
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many deletion |
Multigenic |
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Under unbalanced aberration in structure wherein it involves duplication of a segment |
Duplication |
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— Two breakages in one chromosome segment — Segment is flipped 180 and rejoined |
Inversions |
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Types of inversions |
1. Pericentric inversion 2. Paracentric inversion |
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A type of inversion in which there is an involvement of centromere |
Pericentric inversion |
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A type of inversion in which there is no involvement of centromere |
Paracentric inversion |
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Two nonhomologous chromosomes are broken once and segments (acentric) trade places |
Reciprocal Translocations |
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Type of reciprocal translocation in which the arm is breaking off from one chromosome attaches to another chromosome |
Tandem |
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Type of reciprocal translocation in which two acrocentric chromosomes fuse forming a metacentric chromosome and karyotype appears to be monosomic but genome is intact |
Centric fusion (Robertsonian translocation) |
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metacentric chromosome is split into two acrocentrics |
Centric fission |
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Centromere of a metacentric chromosome splits transversely (perpendicular to the chromatids) during mitosis or meiosis |
Isochromosomes |
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It is different from a gene mutation, as this involves a large portion of or multiple genes in the genome. Moreover, the use of a microscope, genetic or molecular analysis or a combination of several techniques helps assess chromosome variation. |
Chromosome mutation |
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Chromosome mutation can be in two forms: namely? |
Aberration in number and Aberration in structure |
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It does not affect the structure of the DNA but the number. A change in the number of DNA molecules results in extra or lacking DNA molecules needed for normal genetic function. |
Mutation in number |
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Aberration in number. Two basic types of chromosome mutation in number includes? |
Aberrant euploidy Aneuploidy |
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Type of chromosome mutation in number wherein there is changes (more or fewer) in whole chromosome set |
Aberrant euploidy |
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Type of chromosome mutations in number wherein it involves changes in parts of chromosome set. |
Aneuploidy |
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possess the normal chromosome set |
Euploid |
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normal euploidy in certain organisms |
Haploidy (n) and diploidy (2n) |
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organisms with more than two chromosome sets |
Polyploids |
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Can be triploid (3n), tetraploid (4n), pentaploid (5n), hexaploid (6n), and others |
Polyploids |
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refers to the chromosome set number, thus, triploidy, tetraploidy, pentaploidy and so on |
Ploidy or ploidy level |
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A diploid organism with only one chromosome set is called a _________. |
Monoploid |
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True or false: Male bees, wasps and ants are naturally tetraploids |
False; they are Monoploids |
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This are common in plants but rare in animals |
Polyploids |
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Polyploidy is present in flatworms, leeches and brine shrimps, and these species reproduce by ____________? |
Parthenogenesis |
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"the production of offspring by a female with no genetic contribution from a male" |
Parthenogenesis |
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These are organisms that possess abnormal chromosome numbers in which it is smaller or greater in number than the normal chromosome number |
Aneuploids |
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- It is the most common cause of aneuploidy. - Happens when the homologous chromosomes failed to segregate normally to opposite poles during meiosis or mitosis |
Nondisjunction |
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True or false: Meiotic nondisjunction is more common than mitotic nondisjunction and may happen either during meiosis I or meiosis II. |
True |
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In Rearrangements or aberration in structure. There are two types of rearrangements, namely? |
Balanced Unbalanced |
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True or false: When DNA breakage happens within genes, there will be a resulting abnormality in gene functions or the formation of a hybrid gene (apposing of two broken sequences) |
True |
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