Replaces accession AI737422
No longer sequences were available. Score E
Sequences producing significant alignments: (Bits) Value
gi|99866732|gb|ABF67945.1| putative Opie4 gag protein [Zea mays] 399 7e-110
gi|17082480|gb|AAL35397.1| Opie2b gag protein [Zea mays] 395 1e-108
gi|33113970|gb|AAP94592.1| retrotransposon Opie-2 [Zea mays] 393 5e-108
gi|99866719|gb|ABF67933.1| Opie3 gag protein [Zea mays] 389 5e-107
gi|99866697|gb|ABF67913.1| Opie2 gag protein [Zea mays] 386 4e-106
gi|18254418|gb|AAL66759.1|AF464738_10 putative pol protein [Zea 382 1e-104
gi|4185310|gb|AAD09017.1| gag protein [Zea mays] 380 3e-104
gi|17082478|gb|AAL35395.1| Opie2a gag protein [Zea mays] 377 3e-103
gi|3645898|gb|AAC49501.1| Gag [Zea mays] 373 4e-102
gi|18254419|gb|AAL66760.1|AF464738_11 putative gag protein [Zea 337 4e-91
gi|74476706|gb|ABA08421.1| Gag [Zea mays] 308 2e-82
gi|18542174|gb|AAL75483.1|AF466202_9 putative pol protein [Zea m 285 2e-75
BLASTn of sequence:
| Accession | Description | Max score | Total score | Query coverage | E value | Max ident | Links |
| AC157776.1 |
Zea mays chromosome 8 BAC clone ZMMBBb0483G05, complete sequence
|
1082 |
3896 |
100% |
0.0 |
95% |
|
| AC165178.2 |
Zea mays clone ZMMBBb-272P17, complete sequence
|
989 |
1415 |
100% |
0.0 |
93% |
|
| AC152495.1 |
Zea mays BAC clone Z486N13, complete sequence
|
932 |
3391 |
100% |
0.0 |
92% |
|
| AF466202.2 |
Zea mays putative pol protein gene, partial cds; and putative gag-pol precursor -orf2, putative Fourf gag/pol protein, putative NADP-dependent malic enzyme, putative argonaute protein, putative pinhead protein, putative pol protein, putative gag protein, putative TNP2, r1-B73 proteins, putative genetic modifier, putative S-receptor kinase, putative aldose reductase-related protein, putative glutathione peroxidase, putative glycerol 3-phosphate permease, putative response regulator, and putative 4-coumarate-CoA ligase-like protein genes, complete cds
|
930 |
2338 |
100% |
0.0 |
92% |
|
| AF466932.1 |
Zea mays clone BAC 206C17, complete sequence
|
918 |
3368 |
100% |
0.0 |
92% |
|
| AF466931.1 |
Zea mays clone BAC 163K15, complete sequence
|
918 |
2459 |
100% |
0.0 |
92% |
|
| AF090447.2 |
Zea mays 22 kDa alpha zein gene cluster, complete sequence
|
906 |
1986 |
99% |
0.0 |
92% |
|
| DQ493649.1 |
Zea mays cultivar Coroico bz locus region
|
894 |
1624 |
100% |
0.0 |
91% |
|
| AC157319.2 |
Zea mays clone ZMMBBb-136E2, complete sequence
|
888 |
1608 |
99% |
0.0 |
91% |
|
| AY664419.1 |
Zea mays cultivar Mo17 locus 9009, complete sequence
|
886 |
4555 |
100% |
0.0 |
96% |
InterPro Scan of sequence:
Related Literature:
Special Feature
Plant Biology
Remarkable variation in maize genome structure inferred from haplotype diversity at the bz locus
( variability | helitrons | retrotransposons | corn )
Qinghua Wang * and Hugo K. Dooner *
*The Waksman Institute, Rutgers, The State University of New Jersey, Piscataway, NJ 08855; and
Department of Plant Biology, Rutgers, The State University of New Jersey, New Brunswick, NJ 08901
Edited by Susan R. Wessler, University of Georgia, Athens, GA, and approved August 1, 2006 (received for review April 17, 2006)
Maize is probably the most diverse of all crop species. Unexpectedly large differences among haplotypes were first revealed in a comparison of the bz genomic regions of two different inbred lines, McC and B73. Retrotransposon clusters, which comprise most of the repetitive DNA in maize, varied markedly in makeup, and location relative to the genes in the region and genic sequences, later shown to be carried by two helitron transposons, also differed between the inbreds. Thus, the allelic bz regions of these Corn Belt inbreds shared only a minority of the total sequence. To investigate further the variation caused by retrotransposons, helitrons, and other insertions, we have analyzed the organization of the bz genomic region in five additional cultivars selected because of their geographic and genetic diversity: the inbreds A188, CML258, and I137TN, and the land races Coroico and NalTel. This vertical comparison has revealed the existence of several new helitrons, new retrotransposons, members of every superfamily of DNA transposons, numerous miniature elements, and novel insertions flanked at either end by TA repeats, which we call TAFTs (TA-flanked transposons). The extent of variation in the region is remarkable. In pairwise comparisons of eight bz haplotypes, the percentage of shared sequences ranges from 25% to 84%. Chimeric haplotypes were identified that combine retrotransposon clusters found in different haplotypes. We propose that recombination in the common gene space greatly amplifies the variability produced by the retrotransposition explosion in the maize ancestry, creating the heterogeneity in genome organization found in modern maize.
Author contributions: H.K.D. designed research; Q.W. performed research; Q.W. and H.K.D. analyzed data; and H.K.D. wrote the paper.