Mouse α -globin Genes and α -Globin-Like Pseudogenes are not Syntenic
A genetic polymorphism for a Bgl I endonuclease site near the α -globin-like pseudogene α -4 of C57BL/6 and C3H/HeN mice was used to show that α -4 was not affected by three independent mutations in which the adult globin genes α -1 and α -2 were deleted. These results indicated that α -4 might not...
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Published in: | Proceedings of the National Academy of Sciences - PNAS Vol. 78; no. 10; pp. 6362 - 6366 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
National Academy of Sciences of the United States of America
01-10-1981
National Acad Sciences |
Subjects: | |
Online Access: | Get full text |
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Summary: | A genetic polymorphism for a Bgl I endonuclease site near the α -globin-like pseudogene α -4 of C57BL/6 and C3H/HeN mice was used to show that α -4 was not affected by three independent mutations in which the adult globin genes α -1 and α -2 were deleted. These results indicated that α -4 might not be located adjacent to the adult α -globin genes on chromosome 11. Restriction endonuclease analysis of DNA of a primary clone of a Chinese hamster-mouse somatic cell hybrid that had lost mouse chromosomes 11 and 18 showed that this clone lacked the adult murine globin genes α -1 and α -2 but it did contain the α -globin-like pseudogenes α -3 and α -4. These results indicated that the adult α -globin genes and α -globin-like pseudogenes are not located on the same chromosome. Similar analyses of several other Chinese hamster-mouse somatic cell hybrids that had segregated other mouse chromosomes indicated that the α -globin-like pseudogenes α -3 and α -4 are located on mouse chromosomes 15 and 17, respectively. These data explain why α -3 and α -4 were not affected by the three independently induced deletion-type mutations that cause α -thalassemia in the mouse. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0027-8424 1091-6490 |
DOI: | 10.1073/pnas.78.10.6362 |