Abstract:
:Pulsed field gradient gel electrophoresis fractionates chromosome-sized DNA molecules from T. brucei. About 60% of the DNA remains in or close to the gel slot (large DNA). There are about three chromosomes of approximately 2 Mb, at least six chromosomes of 200-700 kb, and roughly a hundred mini-chromosomes of 50-150 kb. The basic copy genes for VSGs 118 and 221 reside in large DNA. Their activation by duplicative transposition leads to the appearance of an additional copy in the 2 Mb DNA, showing that activation involves an interchromosomal gene transposition. When gene 221 is activated without duplication, it remains in large DNA, proving that at least two sites for expression of VSG genes exist. In support of this, the mini-exons encoding the 5' 35 nucleotides of VSG messenger RNAs are in large and 2 Mb DNA. The mini-chromosomes hybridize strongly to VSG gene probes and are absent in C. fasciculata. We suggest that their main function is to provide a large pool of telomeric VSG genes.
journal_name
Celljournal_title
Cellauthors
Van der Ploeg LH,Schwartz DC,Cantor CR,Borst Pdoi
10.1016/0092-8674(84)90302-7subject
Has Abstractpub_date
1984-05-01 00:00:00pages
77-84issue
1eissn
0092-8674issn
1097-4172pii
0092-8674(84)90302-7journal_volume
37pub_type
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