Title: Abbo Metallothionein
1DETECTION OF HUMAN METALLOTHIONEIN 1-A
GENEMUTATIONS AMONG INFORMAL GOLD MINING
WORKERSAT ABU HAMAD, SUDAN USING POLYMERASE
CHAINREACTIONRESTRICTION FRAGMENT
LENGTHPOLYMORPHISM
- By
- Mohammed Elnour Ahmmed Abbo.
- B.V.Sc University of Nyala, 2010
- Supervisor
- Dr. Sumaia Mohamed Ahmed Abukashawa.
-
2Introduction
What is Metallothioneins Structure and its
biological functions? Intracellular, low
molecular and cysteine-rich proteins with
molecular weight from 6 to 7 kDa MTs consist of
two binding domains a and ß. N-terminal part of
protein ß-domain three binding places for
divalent ions. C-terminal part of protein
?-domain four binding places for divalent
ions. The most repeated structure motif
cysteine(C)ycysteine(C)-x- cysteine(C).
(C cysteine, S serine, K lysine, G
glycine, A alanine, T threonine, N
asparagine,E glutamic acid, M methionine, P
proline,D aspartic acid, Q glutamine, I
isoleucine)
Content of aminoacids
Figure 2 Structure of Metallothioneins.
Figure 1 Metallothioneins Amino acids contents.
(1)
3Gene expression and Biological functions of
Metallothioneins
1.Cell Proliferation and Apoptosis. 2.Metallothion
eins as scavengers of reactive oxygen species.
3. Homeostasis of Essential Metals. 4.Detoxificat
ion of heavy metals.
- Entering of metal ions into a cell.
- The ions interact with metal synthesis inhibitor
(MTI). - Released metal transcription factor 1 (MTF-1)
binds to metal responsive element (MRE). - Synthesis of mRNA to translate MT.
- MT binds a heavy metal ion, the
MTheavy-metal-ion complex is transported to
kidney or (f) to heavy metal dependent regulation
proteins.
Figure 3 Metallothioneins biological function .
(2)
4Objectives
- The objective of this study is to test the
hypothesis by - (1) Design a study to investigate to what extent
do effect of human Metallothionein 1 A gene
polymorphism in (HgHydra gyrium.) Liquid mercury
exposure toxicity for gold miners in Abu Hamad
Sudan, and Khartoum grouped in metallic mercury
amalgamation and smelting workers. - (2) Look for new genetic variations in MT1A Gene
by use of restriction fragment length
polymorphism as one method used molecular biology
laboratory applications.
Figure 4 Map of Sudan shown () Abu Hamad area
of study.
(3)
5Materials and Methods
- Ethical Clearance Ethical review and consent
approval were obtained from the Ethical Review
Committee of the Faculty of Science, University
of Khartoum (Khartoum-Sudan),Subjects were chosen
based on their exposure to elemental mercury in
civilian artisanal gold mining in Altawaheen area
in River Nile State. History of the subjects
medical tests was obtained from Abu Hamad
hospital in River Nile State. - Primary Data The study utilized quantitative
methods - for data collection, a detailed questionnaire.
- Secondary Data included related activities
information .
Occupation No. Age average (year)
Gold mining workers 30 29.33
Non-gold mining workers 25 28.16
Total 55 57.49
Figure(7) Subjects age Distribution and average.
Clinical signs No. ()
Urinary tract (nephritis) 8 (26.6)
Pulmonary diseases 6 (20)
Neurological (muscle Tremors) 4 (13.3)
Figure(6) Age distribution for case subjects.
Figure(8) Clinical signs for case subjects.
(4)
6Methods of Data Collection
Figure 9 Mercury amalgamation process in water
dips by workers using naked hands and fingers .
Figure 10 Two Workers in field .
(5)
7- Methods of Molecular Investigation
- Selection and design of primers for
metallothionein gene used domain
www.primer3plus.com to amplify the MT-1A gene
coding region based on PubMed database. - Foreword 5? - CTCCCCAGAACCACACACTT - 3?
Reverse 5?- CCCAGCAACTGATTCAGGAT - 3? BLAST on
web domain www.ncbi.nlhm.nih.gov shown in figure
(11)
Figure 11 NCBI Basic Linear Alignment Search
Tool result for submitted Foreword and Reverse
primers.
(6)
8Results
(A)
(B)
Figure 12 (A) 2 Agarose gel stained with
EtBr showing MT-1-A gene PCR product size162
bp in lanes 2 and 3. Lane M showing
DNA molecular marker (1000-100 bp) .
Figure 13 (B) 3 agarose gel stained with
EtBr for PCR product of MT1A polymorphism
after digestion with Hinf1 enzyme lanes
1,2,10show (148 bp) homozygous, lanes 3,4,5,6
show heterozygote (113 bp) , lane 9 is
negative control, lane M showing DNA marker
(700-50 bp) .
(7)
9Distribution of the mutation in study subjects
and control group are shown in figures (14) and
(15). Gold mining workers available for analysis
were 10 heterozygous 33.3 and 20 homozygous
66.6 for the mutation. The gold mining workers
showed new mutation not detected in the control
subjects. The genotype and allele distribution
among gold mining workers could not be detected
because of this new mutation in the gene.
Figure 14 case subjects.
Figure 15 study subjects.
(8)
10Discussions
- Discussion of Results from the Questionnaire
- There is an affect of elemental mercury
exposure associated with nephrotoxicity as
detected in the studied informal gold mining
workers following exposures to elemental mercury.
This is in accordance with previous reported
studies of Tsuji et al., (2003). Absence of
medical tests for urine and hair mercury levels
in hospitals could not allow the correlation with
urinary levels of Hg in workers. - Discussion of Molecular Results
- The hypothesis is tested by DNA genotyping of
informal gold mining workers. - New mutations in MT1A sequence GAATC (G
alteration), cleaved with HinfI, in this study
was detected this demonstrates that gene
mutations may affect subjects by showing various
clinical signs including nephritis, pulmonary
diseases and muscle tremors associated with
elemental mercury exposure. - This study is the first attempt in Sudan of a
group of informal mining workers population that
investigated an association between elemental
mercury and MT1A polymorphism however the sample
size (55 subjects) challenged the study findings
for wild type homozygotes in addition to the
absence of medical tests for urine and hair
mercury levels in hospitals.
(9)
11Conclusions
- From findings of this study it is suggested that
some MT genetic polymorphisms may affect
elemental mercury exposure. - Recommendations
- It is recommended that the Federal Ministry of
Health starts mission teams for gold mining areas
for routine tests for mercury urine and blood
levels. - Ministry of environment should be making campaign
in the areas of gold mining to evaluate hazards
caused by mercury use. - Open new research gate for Metallothioneins genes
in Sudanese population (Metallomics)and MTs
Biomarkers, in addition to Increasing
socio-economic studies and Participation for
UNIDO ,Global Mercury Project GMP needs to be
applied. - Chelating therapy should be available by meso-2,
3-dimercaptosuccinic acid (DMSA). 2,
3-dimercaptopropane-1-sulfonic acid (DMPS). - Introduced of an alternative gold extraction
technology could assist the workers. - Dissemination of information for toxicity effects
of mercury should be done through media press,
radio, television, posters, Education levels
Authorities, community leaders,NGOs .
(10)
12Acknowledgements
-
- My extended thanks to Dr. Mai Abdel Rahman
Alamasri for her enormous support for this
research work, she has been very helpful and kind
with my requests in laboratory related
activities, without her my research could have
never been accomplished. Special thanks are due
to Dr. Hind Mohamed Abu Shama for her efforts in
bioinformatics courses. - I would like to thank all the team working with
at the Genetics Laboratory in the Department of
Zoology, Faculty of Science, University of
Khartoum Mrs Ihsan Taj Alsir, Ms. Amal Gafar
Thanks are extended to Mrs Mawda Taj alsir in
Abu Hamad Hospital.Thanks are also for volunteer
individuals in the Gold mining and extraction,
with special thanks to Mr. Zachariah.I thank all
those who helped me during this research and
preparation of the Dissertation, I appreciate
their tremendous help and encouragement towards
completing this research.
I am grateful my supervisor Dr. Sumaia Mohamed
Ahmed Abukashawa who provided me great guidance
and much needed steps in my research path.
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