The DOI matches its Crossref record.
Population Structure of Wild Musk Shrews (Suncus murinus) in Asia Based on Mitochondrial DNA Variation, with Research in Cambodia and Bhutan
Abstract
The musk shrew (Suncus murinus) is a small mammalian species belonging to Insectivora. It is widely distributed in Asia. To identify the genetic relationship among wild musk shrew populations and examine its migration route, we investigated the populations of Cambodia and Bhutan by using mitochondrial DNA restriction fragment length polymorphism analysis and compared them with other Asian populations previously described. Four haplotypes were detected in Cambodia and eight in Bhutan. A total of 53 haplotypes were detected in Asia and were classified largely into two groups, the Continental and Island types, based on a minimum spanning network. From the distribution of mtDNA types in wild musk shrews, three major population groups are identified in Asia: South Asia, Southeast Asia, and Malay. It is suggested that the Malay population group was a mix of South and Southeast Asian population groups and that this was a contact area of the two groups. In addition, other contact areas between the South and Southeast Asian groups exist in Myanmar, but unlike the Malay, the Myanmar area was the border of these groups.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The Asian house shrew (Suncus murinus) is a ship-borne invasive species that originated in South Asia.
“Finally, the Asian house shrew (Suncus murinus), is also a ship-borne invasive species that originated in South Asia (Yamagata et al. 1995;Kurachi et al. 2007).”
From Across the Indian Ocean: the prehistoric movement of plants and animals (2011) · cites this paper as Kurachi et al. 2007
Citations
Cites
No references could be resolved yet.
Research works printed but not linked: 28
- Brown, W. M., George, M. Jr., and Wilson, A. C. (1979). Rapid evolution of animal mitochondrial DNA. Proc. Natl. Acad. Sci. USA 76:1967–1971. · DOI · Paper page
- Disotell, T. R. (1999). Human evolution: The southern route to Asia. Curr. Biol. 9:R925–R928. · DOI
- Excoffier, L., Smouse, P. E., and Quattro, J. M. (1992). Analysis of molecular variance inferred from metric distances among DNA haplotypes: Application to human mitochondrial DNA restriction data. Genetics 131:479–491. · DOI · Paper page
- Fleischer, R. C., Perry, E. A., Muralidharan, K., Stevens, E. E., and Wemmer, C. M. (2001). Phylogeography of the Asian elephant (Elephas maximus) based on mitochondrial DNA. Evolution 55:1882–1892. · DOI
- Godfrey, H. (2000). The genetic legacy of the Quaternary ice ages. Nature 405:907–913. · DOI
- Gorog, A. J., Sinaga, M. H., and Engstrom, M. D. (2004). Vicariance or dispersal? Historical biogeography of three Sunda shelf murine rodents (Maxomys surifer, Leopoldamys sabanus, and Maxomys whiteheadi). Biol. J. Linn. Soc. 81:91–109. · DOI
- Hasler, M. J., Hasler, J. F., and Nalbandov, A. V. (1977). Comparative breeding biology of musk shrew (Suncus murinus) from Guam and Madagascar. J. Mammal 58:285–290. · DOI
- Heaney, L. R. (1991). A synopsis of climatic and vegetational change in Southeast Asia. Clim. Change 19:53–61. · DOI
- Hutchison, C. A. III, Newbold, J. E., Potter, S. S., and Edgell, M. H. (1974). Maternal inheritance of mammalian mitochondrial DNA. Nature 251:536–538. · DOI
- Ishikawa, A., and Namikawa, T. (1991). Postnatal growth pattern of F1 hybrids of a cross between two strains of large and small musk shrews, Suncus murinus. Exp. Anim. 40:223–230. · DOI
- Ishikawa, A., Akadama, I., Namikawa, T., and Oda, S. (1989). Development of a laboratory line (SRI line) derived from the wild house musk shrews, Suncus murinus, indigenous to Sri Lanka. Exp. Anim. 38:231–237. · DOI
- Ishikawa, A., Yamagata, T., and Namikawa, T. (1991). An attempt at reciprocal crosses between laboratory strains of large and small musk shrews (Suncus murinus): Influence of body weight difference between sexes on mating success. Exp. Anim. 40:145–152. · DOI
- Iyengar, A., Babu, V. N., Hedges, S., Venkataraman, A. B., Maclean, N., and Morin, P. A. (2005). Phylogeography, genetic structure, and diversity in the dhole (Cuon alpinus). Mol. Ecol. 14:2281–2297. · DOI
- Karafet, T. M., Lansing, J. S., Redd, A. J., Reznikova, S., Watkins, J. C., Surata, S. P. K., Arthawiguna, W. A., Mayer, L., Bamshad, M., Jorde, L. B., and Hammer, M. F. (2005). Balinese Y-chromosome perspective on the peopling of Indonesia: Genetic contributions from pre-Neolithic hunter-gatherers, Austronesian farmers, and Indian traders. Hum. Biol. 77:93–114. · DOI
- Kashiwaya, K., Ochiai, S., Sakai, H., and Kawai, T. (2001). Orbit-related long-term climate cycles revealed in a 12-Myr continental record from Lake Baikal. Nature 410:71–74. · DOI
- Louch, C. D., Ghosh, A. K., and Pal, B. C. (1966). Seasonal changes in weight and reproductive activity of Suncus murinus in West Bengal, India. J. Mammal 47:73–78. · DOI
- Macaulay, V., Hill, C., Achilli, A., Rengo, C., Clarke, D., Meehan, W., Blackburn, J., Semino, O., Scozzari, R., Cruciani, F., Taha, A., Shaari, N. K., Raja, J. M., Ismail, P., Zainuddin, Z., Goodwin, W., Bulbeck, D., Bandelt, H. J., Oppenheimer, S., Torroni, A., and Richards, M. (2005). Single, rapid coastal settlement of Asia revealed by analysis of complete mitochondrial genomes. Science 308:1034–1036. · DOI · Paper page
- McElroy, D., Moran, P., Bermingham, E., and Kornfield, I. (1992). REAP: An integrated environment for the manipulation and phylogenetic analysis of restriction data. J. Hered. 83:157– 158. · DOI
- Nei, M., and Miller, J. C. (1990). A simple method for estimating average number of nucleotide substitutions within and between populations from restriction data. Genetics 125:873–879. · DOI
- Nei, M., and Tajima, F. (1981). DNA polymorphism detectable by restriction endonucleases. Genetics 97:145–163. · DOI
- Tamura, K., and Aotsuka, T. (1988). Rapid isolation method of animal mitochondrial DNA by the alkaline lysis procedure. Biochem. Genet. 26:815–819. · DOI
- Tsubota, Y., Namikawa, T., and Nishida, T. (1986). Morphology and reproduction of wild musk shrews, Suncus murinus, in Sri Lanka. Rep. Soc. Res. Native Livestock 11:241–250.
- Voris, H. K. (2000). Special paper 2, Maps of Pleistocene sea levels in Southeast Asia: Shorelines, river systems, and time durations. J. Biogeog. 27:1153–1167. · DOI · Paper page
- Yamagata, T., Ohishi, K., Faruque, M. O., Masangkay, J. S., Ba-Loc, C., Vu-Binh, D., Mansjoer, S. S., Ikeda, H., and Namikawa, T. (1995). Genetic variation and geographic distribution of the mitochondrial DNA in local populations of the musk shrews, Suncus murinus. Jpn. J. Genet. 70:321–337. · DOI · Paper page
- Yamagata, T., Nakai, K., Tanaka, K., Namikawa, T., Yamamoto, Y., Son, H. V., Ba-Loc, C., Nam, N. H., and Vu-Binh, D. (1999). Morphology and mitochondrial DNA variation of the wild musk shrews in Vietnam. Rep. Soc. Res. Native Livestock 17:179–185.
- Yamagata, T., Kurachi, M., Tanaka, K., Maeda, Y., Nay, W., Than, H., Than, D., and Maung, M. N. (2004). Genetic differentiation of wild musk shrews in Myanmar based on morphology and mitochondrial DNA variation. Rep. Soc. Res. Native Livestock 21:257–266.
- Yong, H. S. (1971). Chromosome polymorphism in the Malayan house shrews, Suncus murinus (Insectivora, Soricidae). Experientia 27:589–591. · DOI
- Yosida, T. H. (1982). Cytogenetical studies on Insectivora II: Geographical variation of chromosomes in the house shrew, Suncus murinus (Soricidae), in East, Southeast and Southwest Asia, with a note on the karyotype evolution and distribution. Jpn. J. Genet. 57:101–111. · DOI
Cited by
Sorted by citations
Across the Indian Ocean: the prehistoric movement of plants and animals
Fuller, D. Q., Boivin, N., Hoogervorst, T., & Allaby, R. (2011) · Antiquity · doi:10.1017/s0003598x00067934 · Cited by 328
East Africa and Madagascar in the Indian Ocean world
Boivin, N., Crowther, A., Helm, R., & Fuller, D. Q. (2013) · Journal of World Prehistory · doi:10.1007/s10963-013-9067-4 · Cited by 232
East African origins for Madagascan chickens as indicated by mitochondrial DNA
Herrera, M. B., Thomson, V. A., Wadley, J. J., Piper, P. J., Sulandari, S., Dharmayanthi, A. B., Kraitsek, S., Gongora, J., & Austin, J. J. (2017) · Royal Society Open Science · doi:10.1098/rsos.160787 · Cited by 28
Metadata
- Authors
- Kurachi, M., Chau, B.-L., Dang, V.-B., Dorji, T., Yamamoto, Y., Nyunt, M. M., Maeda, Y., Chhum-Phith, L., Namikawa, T., & Yamagata, T.
- Venue
- Biochemical Genetics
- Published
- 2007-02-22
- Volume
- 45
- Issue
- 3-4
- Pages
- 165-183
- ISSN
- 0006-2928
- 1573-4927
- Cited by
- 15
- References
- 0
- Language
- en
- Licence
- www.springer.com/tdm (tdm)
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review