These aquaculture-
and conservation-oriented
commentaries are not abstracts written by the original authors.
They reflect the opinions of someone else -- usually Roger Doyle. Direct quotations from the papers or
abstracts are marked with inverted commas.
310. Shrimp markers, shrimp map
Genetic mapping of
the black tiger shrimp Penaeus monodon with amplified fragment length
polymorphism. 2002. Wilson, K., Y. Li, V. Whan, S. Lehnert, K. Byrne,
S. Moore, S. Pongsomboon, A. Tassanakajon, G. Rosenberg, E. Ballment, Z.
Fayazi, J. Swan, M. Kenway, and J. Benzie. Aquaculture 204 (3-4):297-309.
Twenty-three AFLP primers
were used to find 673 polymorphic loci which were free from significant
segregation distortion. Of these marker loci, 116 which were found to be
segregating in more than one of the experimental families were used to
construct a low density linkage map. Some microsatellite loci were also
used. Twenty distinct linkage groups were identified. There are, however,
more than 40 chromosome pairs in P. monodon and the authors say
that there are other large gaps in their preliminary map.
This looks like the start
of a serious mapping program, and it is.
The authors invite contributions from other researchers who have markers
that can be placed on the P. monodon map. The Shrimp-Map project
has a website: http://www.aims.gov.au/pages/research/shrimpmap/pages/sm-00.html . Presumably details on the mapped primers and microsatellites are freely
available from the site or from the authors although I haven't checked. k.wilson@aims.gov.au
or yutao.li@li.csiro.au .
309. Oops! Sorry! Not eureka!
Population
admixture may appear to mask, change or reverse genetic effects of genes
underlying complex traits. 2002. Deng, H.-W. Genetics 159:1319-1323.
If you find a statistical
association between a molecular marker and disease susceptibility or
resistance in a single generation of an aquaculture broodstock, the association will almost
always be false. This is because aquaculture broodstocks usually consist
of relatively few groups of siblings and/or admixed populations which have
somewhat different marker gene frequencies.
The author of this paper
published a useful analysis a year ago (Mar-April 2001 #182) which showed
that when populations mixtures are used to search for QTLs you get a lot
of false positive associations, and you may go chasing after genes that
aren't there.
The new paper goes
further in analysing "the effects and the conditions of population
admixture in masking, changing, or even reversing true genetic effects of
genes underlying complex traits".
The possible solutions
include controlled breeding and progeny testing etc., or doubled
haploid trickery (May 2000 #59, Jan 2002 #279), or perhaps even work in
silico (Aug 2001 #217). deng@creighton.edu .
308. Aureus has two sex chromosomes!
Identification of
putative sex chromosomes in the blue tilapia, Oreochromis aureus, through
synaptonemal complex and FISH analysis. 2001. Campos-Ramos, R. , S.C.
Harvey, J.S. Masabanda, L.A.P. Carrasco, D.K. Griffin, B.J. McAndrew, N.R.
Bromage, and D.J. Penman. Genetica 111 (1-3):143-153.
In O. aureus the
heterogametic sex is thought to be female, unlike O. niloticus, O.
mossambicus and H. sapiens where it is the male, most of the time. In
tilapias the heterogametic sex chromosomes cannot be distinguished by
their appearance as seen through a microscope. This paper is based on a
wonderful optical and electron microscopic study of that magical meiotic moment
when homologous chromosomes are tightly paired and
exchange of genetic material between paired DNA molecules is taking place.
Pairing and exchange does not occur between non-homologous chromosome
regions, and the authors noted two unpaired regions in nuclei of female O
aureus.
The two regions were on
different chromosomes, one of which has not yet been identified in the
karyotype. There were no unpaired regions in aureus males. One of the
unpaired regions is closely related to the sex-determining region of male
niloticus which, however, has only one such region. This paper appears to
be the first demonstration of two pairs of probable sex chromosomes in a
single species. Therefore it is hardly surprising that species hybrids involving
aureus have sex ratios which are strange and unpredictable, but sometimes
useful, not only in the F1 but in descendent generations as well. d.j.penman@stir.ac.uk .
307. One immigrant per generation will not
prevent inbreeding
Migration and
inbreeding: the importance of recipient population size for genetic
management. 2001. Vucetich, J.A., and T.A. Waite. Conservation
Genetics 2 (2):167-171.
This paper makes the
useful point that in real populations the number of immigrants needed to
prevent inbreeding is actually much greater than one individual per
generation, which is the theoretical requirement in idealized
Fisher-Wright populations.
In random-mating
populations where reproductive variance follows a Poisson distribution one
immigrant per generation will theoretically do the trick if the numerical
population size is larger than about 20. However, variation in mating
success, fecundity etc in real populations increases reproductive variance
and causes the effective population size to be considerably less than the
numerical (census) size.
This may be well known,
but the authors point out that the reproductive variance of immigrants
is highly variable as well. The result is that more than one immigrant
individual is needed to prevent inbreeding and the situation becomes worse
the greater the discrepancy between actual and effective population sizes.
Most importantly, the required number of immigrants increases with the
census size of the population, which is not the case in idealized,
theoretical populations in which the census and effective sizes are equal.
It is interesting to
compare this theoretical study with a field study of the effect of a
single immigrant on a bottlenecked population of warblers (Sep 2001 #235).
In that real-world population, selection (purging) apparently removed the
alleles responsible for inbreeding depression, but the immigrant promptly brought
deleterious alleles back in again! javuceti@mtu.edu .
306. Cost-effective breeding design for
aquaculture genetics?
Polymix
breeding with parental analysis of progeny: an alternative to full-sib
breeding and testing. 2001. Lambeth, C., B.-C. Lee, D. O'Malley, and
N. Wheeler. Theoretical and Applied Genetics 103 (6/7):930-943.
This forest genetics
paper describes a simple breeding design for estimating breeding values
that might be directly transferred to aquaculture. Just mix pollen (sperm)
from a lot of males together and fertilize some females with the mixture.
Then use DNA markers to sort out the pedigrees, and use the resulting
relationship matrix and performance data to estimate breeding values of
either the parents or the offspring. The paper has a lot of technical analyses
of statistical power and efficiency, but
basically, what could be easier than this? One major
complication is the variance in reproductive success in aquaculture (#304,
below) which might greatly increase the number of DNA analyses required to
complete the genetic analysis of the polymix offspring. clem.lambeth@weyerhaeuser.com .
305. Markers identify individual shellfish
larvae
Microsatellite
genotyping of individual abalone larvae: parentage assignment in
aquaculture. 2001. Selvamani, M.J.P., S.M. Degnan, and B.M. Degnan.
Marine Biotechnology 3:478-485.
PCR procedures are
sensitive enough so ten microsatellite loci can be analysed on each
veliger larva. Five were used for parentage analysis and three loci were
generally sufficient to assign parentage in this experiment. This can be an efficient way to set up a genetics program in aquaculture. The
authors found, moreover, that most fertilizations were attributable to
just one of the males in the sperm mix. See Nov 2001 #259 on extreme
reproductive variance in elm-oyster species, and the comment in #306,
above, on the complications this might cause in "polymix" mating
designs. bdenan@zoology.uq.edu.au .
304. Variable oyster reproduction decreases
effective population number
High variance in
reproductive success of the Pacific oyster (Crassostrea gigas, Thunberg)
revealed by microsatellite-based parentage analysis of multifactorial
crosses. 2002. Boudry, P., B. Collet, F. Cornette, V. Hervouet, and F.
Bonhomme. Aquaculture 204 (3-4):283-296.
The authors of this paper
used a single, highly variable, microsatellite locus to trace the sources
of variation in the reproductive success of laboratory crosses of C.
gigas. "Results show large variance in parental contributions at
various developmental stages, leading to a strong reduction of
experiment-wide effective population sizes. Segregation distortions
fluctuating with time were also observed. ... observed variance in
reproductive success can be attributed to three main factors: gamete
quality, sperm-egg interaction and differential viability among
genotypes." The authors also found that sperm competition increased
reproductive variance and decreased effective population size.
These results are
qualitatively similar to another recent paper on the same species (Nov
2001 #259). Paper #259 elegantly wrapped developmental mortality,
segregation distortion, inbreeding depression and compulsory sex into a
general theory of life history strategies known as Williams's elm-oyster
model. Elm-oyster species produce enormous numbers of offspring which they
broadcast into a hostile world. The outlook for any particular larva is not good, not least because it usually has a
genotype which is unfit everywhere.
The practical implication
for maintaining diversity in hatcheries is evident. Effective
population number will be particularly hard to maintain in elm-oyster
species. The danger of inbreeding depression will be particularly severe
because (a) it is likely to happen and (b) when it does happen it will
cause serious problems. pboudry@ifremer.fr
303. Marker relatedness estimator agrees
with a very long pedigree record
Microsatellite
diversity, pedigree relatedness and the contributions of founder lineages
to thoroughbred horses. 2001. Cunningham, E.P., J.J. Dooley, R.K.
Splan, and D.G. Bradley. Animal Genetics 32 (6):360-364.
Thoroughbred horse
pedigrees extend back about 300 years and offer a good opportunity to
check the accuracy of marker-based relatedness estimators (Sep 2001 #227).
This paper used a shared-allele estimator calculated from data on twelve
microsatellite loci. Agreement between relatedness calculated from
pedigree records and estimated from the microsatellites was excellent. The
correlation between the recorded pedigrees and relatedness estimators is
good news for aquaculture and fisheries conservation, where pedigrees are
rare and expensive to maintain. Marker-based relatedness estimators may
come into use for estimating variance components (Aug 2000 #88) and
inbreeding (Dec 2001 #269) and for preserving founder diversity in
hatcheries (Nov 2001 #261; Jan 2002 #283). epcnnghnn@tcd.ie
302. More natural selection for MHC
diversity in salmon
Geographic
heterogeneity in natural selection on an MHC locus in sockeye salmon. 2001. Miller, K.M., K.H. Kaukinen, T.D. Beacham, and R.E. Withler.
Genetica 111 (1-3):237-257.
It is becoming evident
that high diversity at the important MHC loci is often, or usually,
maintained by modes of selection that favour diversity per se rather than particular alleles. These selection modes include mate choice
(Jul-Aug 2001 #221) and possibly overdominant selection for disease
resistance (October 2001 #240). This study of 31 populations of sockeye
salmon, like another recent study on Atlantic salmon (December 2001 #272),
demonstrates that balancing selection which increases diversity takes
place locally, within populations.
There is however also evidence for
directional selection at the MHC in several of these sockeye populations.
The Atlantic salmon study found that genetic distances between populations
as measured at the MHC locus correlated reasonably well with genetic
distances measured at neutral microsatellite loci and also with geographic
distance. The Atlantic authors concluded that divergence of populations is
essentially a random process.
The sockeye authors reach
a different conclusion. "The apparent heterogeneity in selection [at
MHC loci] resulted in strong genetic differentiation between
geographically proximate populations with and without detectable levels of
balancing selection, in stark contrast to observations at neutral
loci." The paper finishes with "The distribution of MHC class II
diversity throughout the Fraser drainage supports the contention that
conservation of sockeye salmon must be conducted on the basis of
individual lake systems." Millerk@pac.dfo-mpo.gc.ca .
301. Selection for larval behaviour changes
adult traits
The effects of
selection for larval behavior on adult life-history features in Drosophila
melanogaster. 2001. Foley, P.A., and L.S. Luckinbill. Evolution 55
(12):2493-2502.
Domestication selection
on larval feeding behaviour undoubtedly takes place in hatcheries operated
both for aquaculture and genetic conservation. Presumably hatchery
selection favours larvae that eat more and faster, although that may not
be the case in some culture systems. Anyway we know essentially nothing
about what the genetic consequences of such selection might be, which is
why this experiment on Drosophila is interesting as a model.
The authors found a
tradeoff between fitness traits. Lines selected for high feeding rates as
larvae grew faster but had reduced life spans. Lines selected for a low
larval feeding rate grew more slowly to adulthood but had lower
mortalities and also enhanced expression of genes known to promote
resistance to stress. This may be interesting (by analogy) in the light of
possible growth-survival tradeoffs which has been reported in shrimp (e.g.
Feb 2002 #290). lluckin@biology.biosci.wayne.edu
300. Relaxing intensity of selection does
indeed reduce fitness
The relative
effects of mutation accumulation versus inbreeding depression on fitness
in experimental populations of the housefly. 2001. Reed, D.H., and E.H.
Bryant. Zoo Biology 20 (3):145-156.
The authors of this paper
bred large (500) and small (50) replicate housefly population in a regime
which eliminated selection on traits that are expressed after 21 days of
age. They accomplished this by killing all the flies at 21 days. This is a
useful model experiment for aquaculture or genetic conservation because,
when breeding captive populations, it is hard to know which of several
potential genetic problems to worry about most. Here are three major
worries (which does not however exhaust the list of possible worries):
Worry #1:
deliberate or incidental selection may change the value of traits away
from their natural optima (domestication selection).
Worry #2: Reduced
natural selection in the benign, domestic environment, will permit
unfavorable genes to accumulate in the population by drift and/or mutation
pressure even though they are not selected (relaxed selection). The result
may be a catastrophic loss of fitness when the organisms are exposed again
to the full force of natural selection, e.g. in fisheries
stock-enhancement or in some types of aquaculture. Note that both of these
effects (worry #1 and worry #2) can occur in captive populations of any
size.
Worry #3: If the
captive population is small, inbreeding accumulates as the generations
pass. This occurs because the small sample of gametes in each generation
leads rapidly to the accumulation of deleterious homozygotes – unless
they are purged by selection. See "mutational meltdown" February
2001 #171, "extinction vortex" June 2001 #210; and the unusual
theoretical perspective provided by January 2001 #157.
This model experiment
with a small, captive population of flies provides a useful reality check.
" [The] rate of loss [of later-life fitness components] due to
relaxed selection was equivalent to the rate of loss due to inbreeding in
populations with an effective size of 50 individuals. Even if captive
populations are kept large to avoid inbreeding, breeding them in benign
environments where the forces of natural selection are curtailed may
jeopardize the capability of these populations to exist in natural
environments within few generations." ebryant@fone.net
299. Lonely, crooked, depressed, and
venomous
Low genetic diversity
threatens imminent extinction for the Hungarian meadow viper (Vipera
ursinii rakosiensis). 2002. Újvári, B., T. Madsen, T. Kotenko, M.
Olsson, R. Shine, and H. Wittzell. Biological Conservation 105127-130 (1).
This is a good example of
what can happen to the genetics of small, isolated, remnant populations.
When compared with much larger populations in Ukraine, the Hungarian snakes
have low MHC variability (presumably reducing the immune response), and
greater genetic uniformity. "In combination with reports of birth
deformities, chromosomal abnormalities and low juvenile survival, these
data strongly suggest that the Hungarian vipers are experiencing
inbreeding depression.... Given the very low numbers of animals, the only
feasible strategy to increase the genetic diversity and to save the
Hungarian vipers from extinction is to implement a captive breeding
program based on genetically screened animals." thomas.madsen@zooekol.lu.se.
298. Successful mass selection for growth
in aquaculture
Stock improvement of
silver barb (Barbodes gonionotus Bleeker) through several generations of
genetic selection. 2002. Hussain, M.G., M.S. Islam, M.A. Hossain, M.I.
Wahid, A.H.M. Kohinoor, M.M. Dey, and M.A. Mazid. Aquaculture 204
(3-4):469-480.
Mass selection was
performed on a composite base population which consisted of reciprocal
crosses among fish originating from Thailand, Indonesia and Bangladesh.
The pure Bangladesh stock was used as an unselected reference population.
"A 7.5% genetic gain in growth performance was attained by the F1
crossbred group over the nonselected control group. ...The weight gain
values of the third generation of the selected group showed 21.9%
superiority over the nonselected control." It is nice to see a report
on mass selection that actually works with a tropical fish species.
Hussain e-mail fsbfri@bdonline.com .
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