An unstable allele at the maize Opapue2 locus is caused by the insertion of a double Ac element

1994 ◽  
Vol 243 (3) ◽  
pp. 334-342 ◽  
Author(s):  
D. Michel ◽  
F. Salamini ◽  
M. Motto ◽  
H. P. Döring
Keyword(s):  

1988 ◽  
pp. 213-226 ◽  
Author(s):  
Hugo K. Dooner ◽  
Edward Ralston ◽  
James English
Keyword(s):  


Genetics ◽  
1992 ◽  
Vol 130 (2) ◽  
pp. 377-384 ◽  
Author(s):  
G Baran ◽  
C Echt ◽  
T Bureau ◽  
S Wessler

Abstract The somatic and germinal behavior of the maize wx-B3 mutation indicates that this Ac allele rarely reverts. Endosperms containing wx-B3 display tiny and infrequent Wx revertant sectors while no significant reversion is detected when wx-B3 pollen is stained with I/KI. Previous studies of other transposable element alleles that revert infrequently have implicated low levels of element excision. Unlike these other alleles, the wx-B3 Ac element is indistinguishable from fully active Ac elements with respect to its structure, and its ability to transpose from the Wx gene or to trans-activate a Ds element. Characterization of somatic and germinal excision events lead us to conclude that excision of the wx-B3 Ac element almost always produces null alleles. Furthermore, the excellent correlation between the position of the wx-B3 mutation on the physical and genetic maps indicates that the Ac insertion is the only lesion of wx-B3. As a result, precise excision of this Ac should restore Wx function. The fact that revertant sectors and pollen grains are rare indicates that precise excision of Ac is also rare. The finding that the wx-B3 reversion frequency is comparable whether wx-B3 is hemizygous or over a wx allele with a wild-type insertion site illustrates a fundamental difference between the excision mechanisms of Ac and Drosophila P elements.



2005 ◽  
Vol 133B (1) ◽  
pp. 124-126 ◽  
Author(s):  
Quasar Saleem Padiath ◽  
Achal Kumar Srivastava ◽  
Sanghmitra Roy ◽  
Satish Jain ◽  
Samir Kumar Brahmachari


1988 ◽  
Vol 79 (3) ◽  
pp. 147-150 ◽  
Author(s):  
M. A. L. Smith ◽  
L. A. Spomer ◽  
R. K. D. Cowen


Genetics ◽  
2004 ◽  
Vol 167 (4) ◽  
pp. 1929-1937 ◽  
Author(s):  
Jianbo Zhang ◽  
Thomas Peterson


Genetics ◽  
1991 ◽  
Vol 128 (1) ◽  
pp. 163-173 ◽  
Author(s):  
P Athma ◽  
T Peterson

Abstract The maize P gene conditions red phlobaphene pigmentation to the pericarp and cob. Starting from two unstable P alleles which carry insertions of the transposable element Ac, we have derived 51 P null alleles; 47 of the 51 null alleles have a 17-kb deletion which removes the 4.5-kb Ac element and 12.5 kb of P sequences flanking both sides of Ac. The deletion endpoints lie within two 5.2-kb homologous direct repeats which flank the P gene. A P allele which contains the direct repeats, but does not have an Ac insertion between the direct repeats, shows very little sporophytic or gametophytic instability. The apparent frequency of sporophytic mutations was not increased when Ac was introduced in trans. Southern analysis of DNA prepared from the pericarp tissue demonstrates that the deletions can occur premeiotically, in the somatic cells during development of the pericarp. Evidence is presented that the deletions occurred by homologous recombination between the two direct repeats, and that the presence of an Ac element at the P locus is associated with the recombination/deletion. These results add another aspect to the spectrum of activities of Ac: the destabilization of flanking direct repeat sequences.



1991 ◽  
Vol 11 (12) ◽  
pp. 6192-6196
Author(s):  
S R Wessler

The null wx-ml allele contains a 409-bp Dissociation 1 (Ds1) element in exon 9 of the maize waxy (Wx) gene. In the absence of the autonomous Activator (Ac) element, the Ds1 element cannot transpose, and this allele encodes several Wx transcripts that arise following alternative splicing of Ds1 sequences from Wx pre-mRNA. Splicing involves the utilization of three 5' splice sites and three 3' splice sites. All but one of these splice sites are in Ds1 sequences near the ends of the element. The presence of 5' and 3' splice sites near the Ds1 termini and the element's small size and AT richness are features that distinguish Ds1 elements from all other known Ds elements. It is suggested that these features may enhance the ability of Ds1 to function as a mobile intron.



1993 ◽  
Vol 90 (20) ◽  
pp. 9693-9697 ◽  
Author(s):  
P. W. Atkinson ◽  
W. D. Warren ◽  
D. A. O'Brochta


Genetics ◽  
1981 ◽  
Vol 98 (2) ◽  
pp. 291-302
Author(s):  
John D Raymond ◽  
Michael J Simmons

ABSTRACT The behavior of an unstable allele of the singed-bristle locus on the X chromosome was studied in connection with the occurrence of lethal mutations on that same chromosome. The unstable allele, weak singed (snw), is under the control of the P-M system of hybrid dysgenesis and, in the M cytotype, mutates secondarily to extreme singed (sne) and to wild type (sn  +) at high rates. Chromosomes whose snw allele had mutated in this fashion sustained lethal mutations at a rate of 3%; whereas, those whose snw allele had apparently remained unchanged, acquired lethals at a lower rate, 1.3%. The significant difference between these values indicates a statistical coincidence between the phenomena of snw instability and X-linked lethal mutation induction. This coincidence can be explained by postulating that mutations at the singed locus sometimes release a genetic element capable of reinserting elsewhere in the chromosome. Alternately, snw instability and lethal induction might be associated because they are the effects of a common cause, perhaps some mutation-inducing substance present in various amounts in the germ cells of dysgenic flies.—The lethals that occurred on chromosomes whose snw allele had mutated to sne mapped preferentially close to singed. The lethals on the snw and sn  + chromosomes did not show this concentration on the map. Cytological analysis of samples of all three types of lethal chromosomes indicated that, with one exception, there was no detectable breakage at the singed locus itself. The single instance of breakage at singed was not associated with any change in the singed phenotype. Thus, the instability of snw apparently does not involve detectable breakage of the singed locus, or if it does, this breakage is not a common event.



1991 ◽  
Vol 16 (2) ◽  
pp. 369-371 ◽  
Author(s):  
Reinhard Hehl ◽  
Wolfgang K. F. Nacken ◽  
Andrea Krause ◽  
Heinz Saedler ◽  
Hans Sommer


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