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The Chromosomal Basis of Inheritance
The Chromosomal Basis of Inheritance

... (recombination frequency) depends on the distance between genes on a chromosome  assumed crossing over a random event, equally likely to occur anywhere along length of a chromosome ...
Dave Cooke Mitosis
Dave Cooke Mitosis

... spindle fibers attach to centromeres  creating kinetochores ...
Genetics Reference Sheet
Genetics Reference Sheet

... allele combinations Dominant trait- An allele that expresses its phenotypic effect even when heterozygous with a recessive allele (the big guy always wins) Recessive trait- allele that does not express a characteristic effect when present with a dominant allele. Expresses only when 2 recessive allel ...
Genetics Practice Problems - juan-roldan
Genetics Practice Problems - juan-roldan

... A) Male and female gametes are produced in separate organs in separate individuals. B) There are two chromosome divisions in meiosis. C) Recombination (crossing over) occurs in meiosis. D) Homologous chromosomes are randomly separated during meiosis I. E) Sister chromatids do not separate until meio ...
Which best describes an allele? (A) a physical trait
Which best describes an allele? (A) a physical trait

... recessive offspring. This is better than (A) crossing him with another heterozygous dog in a monohybrid cross, because there’s only have a 25% of producing homozygous offspring. That means if the offspring all have black fur, you can say the dog is homozygous dominant with more certainty in a cross ...
Klinefelter’s syndrome is caused by a nondisjunction event
Klinefelter’s syndrome is caused by a nondisjunction event

... a nondisjunction event during meiosis 1. A gamete ends up with two sex chromosomes, and when the two sex chromosomes of one parent are added to the one of the other it causes a trisomy in their offspring. Because it is caused by nondisjunction, the disorder is neither dominant or recessive. ...
Sex-Linked Genes - Mr. Kleiman`s Wiki
Sex-Linked Genes - Mr. Kleiman`s Wiki

... Below is a human ___________________. This is a picture of all of the chromosomes in one human cell. All cells in the body of one individual (except in the gametes) will have this same set of chromosomes. Unsorted Chromosomes ...
Post Review of Mid-Term - Rutherford County Schools
Post Review of Mid-Term - Rutherford County Schools

... Anaphase – Chromosomes move AWAY to opposite poles Telophase – TWO nuclear envelopes ...
UNIT 6 STUDY GUIDE
UNIT 6 STUDY GUIDE

... Are cells produced diploid or haploid? Does crossing over occur? If crossing over does occur, WHEN does it happen? What is the reason or purpose for producing the daughter cells? (what are they used for?) How similar are the daughter cells to the parent cells? How similar are the daughter cells to e ...
Domain Three (3_genetics)
Domain Three (3_genetics)

... A. Both eggs and sperm cells have the same number of chromosomes. B. Both eggs and sperm cells have one-half the parent cells' chromosome number. C. It is a process producing gametes only. D. It is the same process that occurs in body cell division. 12. An egg and a sperm cell each have 16 chromosom ...
What makes us human?
What makes us human?

... • By the way, this is one way to tell the sex of a cat. If the cat’s fur has three colors—white with orange and black spots, for example—you can almost be certain that it is female. ...
Reproductive Physiology
Reproductive Physiology

... – Results in the formation of secondary oocytes – These are dictyate in prophase I ...
I. Types of Genetic Disorders
I. Types of Genetic Disorders

... • Diseases caused by alleles on sex chromosomes • Autosomal Dominant • Diseases caused by dominant alleles • Autosomal Recessive • Diseases caused by recessive alleles ...
Section 1: Mendelʼs Work * Gregor Mendel was a young priest from
Section 1: Mendelʼs Work * Gregor Mendel was a young priest from

... * He noticed that sometimes the traits of the offspring pea plants were similar to the parents and then other times they were different. The passing of traits from parents to offspring is known as HEREDITY. * Over the course of ten years, he experimented, studied, and documented thousands of pea pla ...
Chapter 10
Chapter 10

... C. X-linked genes have unusual inheritance patterns 1. The Y chromosome contains few, but important, genes for maleness, such as the srY gene (sex-reversal on Y) a) This gene causes other genes to "turn on," resulting in male characteristics in the embryo 2. Genes located on the X chromosomes are ca ...
More detail on linkage and Morgan
More detail on linkage and Morgan

... • In humans, the anatomical signs of sex first appear when the embryo is about two months old. • In individuals with the SRY gene (sex-determining region of the Y chromosome), the generic embryonic gonads are modified into testes. – Activity of the SRY gene triggers a cascade of biochemical, physiol ...
Histone depleted metaphase chromosomes Scaffold Attachment
Histone depleted metaphase chromosomes Scaffold Attachment

... • Previously it was predicted that active genes would be located at the surface of chromosome territories. • Now, it appears that they are also in the interior • Some are also found on loops outside of the territory ...
Slide 1
Slide 1

... • Previously it was predicted that active genes would be located at the surface of chromosome territories. • Now, it appears that they are also in the interior • Some are also found on loops outside of the territory ...
Jeopardy
Jeopardy

... chromosomes (for instance, chromosome 21 in the case of Down syndrome) fails to separate in anaphase I of meiosis. The resulting gametes have an abnormal number (22 or 24) of chromosomes. In plants, an entire set or sets of homologous chromosomes fail to separate, leading to gametes that are 2n or 3 ...
X-inactivation
X-inactivation

... constitutive heterochromatin does not contain any genes facultative: genes are not usually transcribed 7. Heterochromatin does not participate in genetic recombination polymorphism of heterochromatic regions - difficulties in homologous pairing 8. Tendency to agregate during interphase agregation of ...
Automictic and apomictic parthenogenesis in psocids
Automictic and apomictic parthenogenesis in psocids

... It is generally accepted that automixis is not evolutionarily far from normal meiosis and fertilization (SAURA et al. 1993), thus automictic unisexuals can reverse to the normal bisexual state. Conversely, true apomictic parthenogenesis can evolve through the automictic condition and most likely rep ...
BSC1005 /Belk_Chapter 5
BSC1005 /Belk_Chapter 5

...  BRCA2 is a gene that makes a protein that repairs damaged DNA. A mutant version cannot help repair DNA and it will allow the cell to divide with the damage.  Some Characteristics of Normal Cells 1. Normal cells exhibit contact inhibition 2.Normal cells exhibit anchorage dependency 3. Normal cells ...
Patterns of Gene Inheritance
Patterns of Gene Inheritance

...  Individual genes, or DNA segments, contain the genetic blue-print which is ultimately expressed in our hair color, blood type, etc.  DNA is packaged in chromosomes Homologous chromosomes: chromosomes of the same size and shape that contain genes for the same trait  Each somatic cell contains 23 ...
Honors Biology Study Guide for Final Exam
Honors Biology Study Guide for Final Exam

... identify the plant structures that are involved in photosynthesis state the importance of photosynthesis Identify the steps of the light dependent and the light-independent reaction (identify the raw materials needed to start each phase, know the products made by each phase Describe the role of pigm ...
chapter_14_human_heredity
chapter_14_human_heredity

... • Trisomy: Ending up with 3 copies of a chromosome instead of 2. • If a person has 3 copies of chromosome 21, this person has the condition known as Down Syndrome. This occurs in 1 out of 800 babies born. • The main symptoms are mild to moderate mental retardation. ...
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Meiosis



Meiosis /maɪˈoʊsɨs/ is a specialized type of cell division which reduces the chromosome number by half. This process occurs in all sexually reproducing single-celled and multi-celled eukaryotes, including animals, plants, and fungi. Errors in meiosis resulting in aneuploidy are the leading known cause of miscarriage and the most frequent genetic cause of developmental disabilities. In meiosis, DNA replication is followed by two rounds of cell division to produce four daughter cells each with half the number of chromosomes as the original parent cell. The two meiotic divisions are known as meiosis I and meiosis II. Before meiosis begins, during S phase of the cell cycle, the DNA of each chromosome is replicated so that it consists of two identical sister chromatids. In meiosis I, homologous chromosomes pair with each other and can exchange genetic material in a process called chromosomal crossover. The homologous chromosomes are then segregated into two new daughter cells, each containing half the number of chromosomes as the parent cell. At the end of meiosis I, sister chromatids remain attached and may differ from one another if crossing-over occurred. In meiosis II, the two cells produced during meiosis I divide again. Sister chromatids segregate from one another to produce four total daughter cells. These cells can mature into various types of gametes such as ova, sperm, spores, or pollen.Because the number of chromosomes is halved during meiosis, gametes can fuse (i.e. fertilization) to form a zygote with a complete chromosome count containing a combination of paternal and maternal chromosomes. Thus, meiosis and fertilization facilitate sexual reproduction with successive generations maintaining the same number of chromosomes. For example, a typical diploid human cell contains 23 pairs of chromosomes (46 total, half of maternal origin and half of paternal origin). Meiosis produces haploid gametes with one set of 23 chromosomes. When two gametes (an egg and a sperm) fuse, the resulting zygote is once again diploid, with the mother and father each contributing 23 chromosomes. This same pattern, but not the same number of chromosomes, occurs in all organisms that utilize meiosis. Thus, if a species has 30 chromosomes in its somatic cells, it will produce gametes with 15 chromosomes.
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