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GENES AND EXPERIENCE:Genetic Basis of behavior, In breeding

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Neurological Basis of Behavior (PSY - 610)
VU
LESSON 10
GENES AND EXPERIENCE
Objective:
·  To understand the Brain behaviour relationships from the perspectives of biological systems.
In this section of the module the students would go through and understand Biological systems- their
genetic basis and similarities with other animals. Mendelian Genetics. Where is the genetic
programming of behaviour ( if any) Watson Crick Model. What are the similarities and differences
between species, progenies of higher order animals, including homosapien? How much do genes
contribute to behavior: The discipline of Behavior genetics?
Genetic Basis of behavior
Genes not act directly on behaviour, but on the proteins/aminoacids which are responsible for
the structure and metabolism of the organism.
Behavior geneticist and studies in this area agree that a) environment and experience are
important as they interact with genetic material. The researcher try to pinpoint how much of
each contribute to behavior. b) a single gene at a single location cannot lead to one behaviour.
Behavior is the sum total of different genes at different loci. It is not an all or none
characteristics. It is always a combination of different genes, polygenic systems.
Experimental Studies: Genetic Manipulation
There have been experimental studies which manipulate genes using artificial selection and other
conditions in animals reared in labs. This is done because the environmental conditions in the laboratory
are held constant (temperature, day/night cycle , food and the social environment),selection of specific
traits of interest which can be followed up, and animals with those characteristics mated and progenies (
offspring ) followed up and tested for behavioral as well as other characteristics.
How do the behavioural geneticists measure and test behaviour of interest in the laboratory animals. The
characteristics of interest are taken and animals tested and their scores/ performance looked at carefully.
Then animals scoring on both extremes separated form the group that is the High and Low scorers taken
and separated. Then low scorer females and low scorer males mated. The same procedure was carried
out for the high scorers. The progenies were then developed into two separate populations by repeated
selective testing and mating. This has been done as early as in the 1930's.
Tryon ( 1934) carried out an experiment at the University of Berkley where he bred maze bright ( who
did extremely well on maze tests) and maze dull( those who made a lot of errors in maze) rats for 21
generations. By the 8th generation no overlap in two he found that there was no overlap in the two
populations. The question that it could be possibly due to rearing as bright mothers were rearing bright
offspring. This was ruled out as he designed an experimental cross fostering design in which the maze
bright offspring were reared by maze dull parents; they still made significantly less errors. Similarly,
using the same cross fostering procedure he had dull rats reared by bright rats. Since then many
behaviors such as open field activity, alcohol and morphine preference has been identified using such
designs. However we must remember that behaviour is complex, and has multiple variables. There is
not just one single gene for maze running, (there are a lot of cues involved). Further, Searle (1949)
reported that in comparing two groups, he conducted 30 different tests on the maze bright and maze
dull. He reports that maze bright rats were superior in performance and less emotional, therefore the
better learner may learn because there is more emotional stability not because they are more intelligent!
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Neurological Basis of Behavior (PSY - 610)
VU
Are there any Environment effects? Cooper and Zubeck ( 1958) raised the maze bright/dull rats in three
different environments a) impoverished( cage made from wire netting with groups living), b)
stimulating and enriched housing with wire netting, group housing but it had toys, ramps for animals to
play with. His findings showed that the maze dull rats perform similar to the maze bright if reared in
stimulating environment. Bennett, Diamond, Krech and Rozenweig (1964) found that rats in richer
environment have thicker cortices! This means that their brain development is affected by early
stimulation (more on this later in the chapter on brain development)
The foremost names in the field of genetics and behaviour are Theodosius Dobzhansky and Seymour
Benzer. Their work on Drosophilia (fruitfly) is pioneering work. They took a genetically heterogenous
population and through selective breeding created new breeds to show that behaviour genetically linked.
A lot of work was needed to identify which behaviours were linked to which genes and were located on
which chromosome! Further, constant selection was to be maintained or genetic pool could be broken
into, genes may get re-assorted and effort gone waste (and behaviour under observation may get lost). It
could be a simple careless mistake of a stray fly getting into the experimental breeding cage.
In Dobzhansky and Benzer's experiments, the gene material was also changed through radiation and bio
engineering manipulations. They developed mutants who were sluggish (slow movers) hyperkinetic
(very fast movers, who died soon as they consumed more oxygen and body metabolism faster) non
climbers (those who could not climb against gravity), easily shocked (goes into seizure) negatively
phototactic (those who move away from light source- normal flies move towards light).
Similarly dogs were identified for characteristics by John Paul scott in his laboratory in bar harbor
Maine. The breed beagle (snoopy dog of the cartoons) became the model for hyperactivity.
Mouse strains were identified and bred for different characteristics; aggressive behaviors, alcoholics vs.
nonalcoholic, hoarders vs. non-hoarders, emotionality (defecate in a novel situation), waltzing mice
(inner ear defect). All of this is a consequence of in breeding
In breeding
Simply defined this is repeatedly using the same gene pool which leads to expression of recessive genes
which may carry both behavioural and physical defects.
In a study Theisen (1972) reports that the death rate in children below 10 years of age is 24 per 1000 in
normal population. In interrelated marriages it rises to 81 per 1000. In closer marriages the rate rises
even more. There are other more serious effects such as physically less capable, weaker and age when
they walked and talked was much later than normals. This showed developmental lags. Other deficits
that Theisen (1972) reports are lower Intelligence scores, with lower verbal scores, and language scores
were even lower than normals.
In summary, it is well documented that if the gene pool is reduced more recessive disorders show up.
Larger gene pools lead to a healthier and longer surviving offspring which can compete in a wide range
of environments.
References:
1. Kalat J.W (1998) Biological Psychology Brooks/ Cole Publishing
2. Carlson N.R. (2005) Foundations of Physiological Psychology Allyn and Bacon, Boston
3. Pinel, John P.J. (2003) Biopsychology (5th edition) Allyn and Bacon Singapore
4 Bloom F, Nelson and Lazerson (2001), Behavioral Neuroscience: Brain, Mind and Behaviors (3rd
edition) Worth Publishers New York
5. Bridgeman,B (1988)The Biology of Behaviour and Mind. John Wiley and Sons New York
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Table of Contents:
  1. INTRODUCTION:Descriptive, Experimental and/ or Natural Studies
  2. BRIEF HISTORICAL REVIEW:Roots of Behavioural Neurosciences
  3. SUB-SPECIALIZATIONS WITHIN THE BEHAVIORAL NEUROSCIENCES
  4. RESEARCH IN BEHAVIOURAL NEUROSCIENCES:Animal Subjects, Experimental Method
  5. EVOLUTIONARY AND GENETIC BASIS OF BEHAVIOUR:Species specific
  6. EVOLUTIONARY AND GENETIC BASIS OF BEHAVIOUR:Decent With Modification
  7. EVOLUTIONARY AND GENETIC BASIS OF BEHAVIOUR:Stereoscopic vision
  8. GENES AND EXPERIENCE:Fixed Pattern, Proteins, Genotype, Phenotypic
  9. GENES AND EXPERIENCE:Mendelian Genetics, DNA, Sex Influenced Traits
  10. GENES AND EXPERIENCE:Genetic Basis of behavior, In breeding
  11. GENES AND EXPERIENCE:Hybrid vigor, Chromosomal Abnormalities
  12. GENES AND EXPERIENCE:Behavioral Characteristics, Alcoholism
  13. RESEARCH METHODS AND TECHNIQUES OF ASSESSMENT OF BRAIN FUNCTION
  14. RESEARCH METHODS AND TECHNIQUES OF ASSESSMENT OF BRAIN FUNCTION:Activating brain
  15. RESEARCH METHODS AND TECHNIQUES OF ASSESSMENT OF BRAIN FUNCTION:Macro electrodes
  16. RESEARCH METHODS AND TECHNIQUES OF ASSESSMENT OF BRAIN FUNCTION:Water Mazes.
  17. DEVELOPMENT OF THE NERVOUS SYSTEM:Operation Head Start
  18. DEVELOPMENT OF THE NERVOUS SYSTEM:Teratology studies, Aristotle
  19. DEVELOPMENT OF THE NERVOUS SYSTEM:Stages of development, Neurulation
  20. DEVELOPMENT OF THE NERVOUS SYSTEM:Cell competition, Synaptic Rearrangement
  21. DEVELOPMENT OF THE NERVOUS SYSTEM:The issues still remain
  22. DEVELOPMENT OF THE NERVOUS SYSTEM:Post natal
  23. DEVELOPMENT OF THE NERVOUS SYSTEM:Oxygen level
  24. Basic Neuroanatomy:Brain and spinal cord, Glial cells, Oligodendrocytes
  25. Basic Neuroanatomy:Neuron Structure, Cell Soma, Cytoplasm, Nucleolus
  26. Basic Neuroanatomy:Control of molecules, Electrical charges, Proximal-distal
  27. Basic Neuroanatomy:Telencephalon, Mesencephalon. Myelencephalon
  28. Basic Neuroanatomy:Tegmentum, Substantia Nigra, MID BRAIN areas
  29. Basic Neuroanatomy:Diencephalon, Hypothalmus, Telencephalon, Frontal Lobe
  30. Basic Neurochemistry:Neurochemicals, Neuromodulator, Synaptic cleft
  31. Basic Neurochemistry:Changes in ionic gates, The direct method, Methods of Locating NT
  32. Basic Neurochemistry:Major Neurotransmitters, Mesolimbic, Metabolic degradation
  33. Basic Neurochemistry:Norepinephrine/ Noradrenaline, NA synthesis, Noadrenergic Pathways
  34. Basic Neurochemistry:NA and Feeding, NE and self stimulation: ICS
  35. Basic Neurochemistry:5HT and Behaviors, Serotonin and sleep, Other behaviours
  36. Basic Neurochemistry:ACH and Behaviors, Arousal, Drinking, Sham rage and attack
  37. Brain and Motivational States:Homeostasis, Temperature Regulation, Ectotherms
  38. Brain and Motivational States:Biological Rhythms, Circadian rhythms, Hunger/Feeding
  39. Brain and Motivational States:Gastric factors, Lipostatic theory, Neural Control of feeding
  40. Brain and Motivational States:Resting metabolic state, Individual differences
  41. Brain and Motivational States:Sleep and Dreams, Characteristics of sleep
  42. Higher Order Brain functions:Brain correlates, Language, Speech Comprehension
  43. Higher Order Brain functions:Aphasia and Dyslexia, Aphasias related to speech
  44. Higher Order Brain Functions:Principle of Mass Action, Long-term memory
  45. Higher Order Brain Functions:Brain correlates, Handedness, Frontal lobe