Gene T10P11.15
Identification LUMINIDEPENDENS
Position: 82697 to 87602, from the 5'-UTR through the CDS to the 3'-UTR
Strand +
EST match none
Database match LD gene from A. thaliana cv Wassilewskija

Mutations in the LUMINIDEPENDENS (LD) gene confer a late-flowering phenotype, indicating that LD normally functions to promote the floral transition in Arabidopsis. ld mutants respond normally to changes in photoperiod, and LD mRNA abundance is not affected by these same treatments, suggesting that LD belongs to the autonomous pathway of floral promotion. Several key features of the LD protein, including a putative homeodomain, a glutamine-rich domain, and two bipartite consensus nuclear localization motifs, indicate that LD may function as a transcriptional regulatory protein. We have demonstrated that LD is localized to the nucleus, consistent with its proposed transcriptional regulatory role. The LD transcript accumulates prior to flowering in the vegetative shoot apical meristem (SAM) and after flowering in floral meristems. LD is also expressed in the root meristem of seedlings and in young leaf primordia, but not in mature leaves. LD most likely functions in the SAM to promote flowering; however, we cannot at this point rule out young leaf primordia or roots as a source of LD-derived floral promotion signals. For an extensive discussion on this gene and its role in flowering, please see the article by Lee, et al. (1994 Plant Cell 6:75-83).

The above was kindly provided by Milo Aukerman in the laboratory of Rick Amasino - 16 Oct 97.

The LD gene products of cv Columbia and cv WS are 100% identical, but, interestingly, there are differences in the organization of the LD exons. Columbia exon 4 is split into two exons in WS; while Columbia exons 11 and 12 are joined as a single exon in WS. Thus, the total number of exons in the LD gene is conserved in the two cultivars.

 

mRNA:  Based on a comparison to LD cDNA U03456, the 5'-UTR extends from position 82697 to 82841 and the 3'-UTR resides from position 87439 to 87602.

 

CDS: The table below lists the 13 exons of LD, their coordinates within the BAC, and which exon-finding program(s) predicted the 5' or 3' terminus of that exon (GF = GeneFinder, GS = GenScan, Gr = Grail, M = MZEF, Fe = FEXA, Fg = FGENEA, NPG = NetPlantGene - selects termini only, not exons). The exon coordinates were delineated by a comparison to the published cDNA sequence.

Exon Range 5' 3'
1 82842 to 83006 GF, GS, Gr, Fg, Fe GS, Gr, Fe, NPG
2 83300 to 83327 GF, GS, Gr, Fe, NPG GS, Gr
3 83481 to 83611 GS, M, Gr, Fg, Fe, NPG GF, GS, M, Gr, Fg, Fe, NPG
4 83741 to 84108 GF, GS, M, Gr, Fg, NPG GF, GS, M, Fg, NPG
5 84203 to 84296 GF, GS, M, NPG GF, GS, M, NPG
6 84381 to 84474 GS, Gr, NPG NPG
7 84572 to 84701 NPG NPG
8 84797 to 84830 GS, M, Gr, NPG GS, M, Gr, NPG
9 84906 to 84949 GF, M, Gr, Fg, NPG GF, M, Gr, Fg, NPG
10 85039 to 85127 GF, Gr, NPG GF, Gr, NPG
11 85363 to 85959 GF, NPG GF, GS, M, Gr, NPG
12 86095 to 86609 GF, GS, M, Gr, NPG GF, GS, Gr, NPG
13 86866 to 87438 GF, GS, M, Gr, NPG GF, GS, Gr

 

Complete CDS of LD

ATGGACGCGTTCAAGGAGGAGATAGAAATCGGGAGCTCGGTGGAGTCTTTAATGGAGCTA
TTGGATTCGCAGAAGGTGCTTTTTCATAGCCAGATCGATCAGCTCCAAGATGTCGTCGTT
GCGCAATGCAAACTTACCGGCGTTAATCCCCTTGCGCAAGAAATGGCTGCTGGTGCTTTG
TCCATTAAAATTGGAAAGCGGCCAAGAGACTTGTTGAATCCTAAGGCTGTTAAGTATCTA
CAAGCAGTTTTCGCAATTAAAGATGCTATTAGTAAGAGGGAATCTCGGGAGATAAGTGCT
TTATTTGGCATCACAGTCGCCCAGGTTCGAGAATTTTTTGTTACTCAAAAGACAAGAGTG
AGGAAACAGGTGAGGCTTTCAAGGGAGAAAGTAGTTATGTCCAATACGCATGCTTTACAA
GATGATGGTGTTCCGGAAAATAACAATGCCACAAATCATGTTGAACCCGTTCCCTTGAAC
TCTATACATCCGGAGGCATGTTCTATAAGCTGGGGTGAAGGTGAAACAGTGGCACTTATT
CCACCTGAAGATATTCCACCTGACATCAGCGATTCAGACAAATACTTTGTTGAGAATATA
TTTTCTCTGCTGCGTAAAGAGGAAACATTTTCAGGCCAGGTGAAACTAATGGAGTGGATC
ATGCAGATACAAGATGCTTCTGTGCTGATCTGGTTTTTATCAAAAGGAGGGGTTTTGATA
CTTACAACATGGTTAAGTCAAGCTGCTAGTGAAGAGCAAACAAGTGTCTTACTTCTTATC
CTGAAGGTTCTTTGTCATTTACCTCTCCACAAAGCATCTCCTGAAAATATGTCTGCCATA
TTACAAAGCGTTAATGGACTTCGTTTCTATAGGATATCAGACATATCAAACAGGGCAAAA
GGTTTGTTATCAAGGTGGACCAAGTTATTTGCGAAAATCCAAGCTATGAAGAAACAAAAT
CGTAACAGTTCGCAAATTGATTCGCAGAGTCAATTGCTTCTGAAACAGAGTATTGCTGAA
ATCATGGGTGATAGTAGCAATCCTGAAGATATTCTTAGTCTCTCAAATGGAAAGTCAGAG
AATGTCAGGAGGATTGAATCGTCACAGGGTCCAAAACTGTTGCTTACTTCTGCAGATGAT
TCCACCAAGAAACACATGCTTGGTTCAAATCCATCGTATAACAAAGAACGCAGGAAAGTA
CAGATGGTGGAACAACCAGGCCAAAAAGCTGCTGGAAAGAGTCCGCAGACAGTAAGAATA
GGAACTTCAGGTCGAAGCCGCCCAATGTCTGCTGATGATATTCAGAAAGCAAAGATGCGT
GCCCTTTATATGCAGAGCAAGAACAGTAAAAAGGATCCTTTACCAAGTGCCATTGGTGAT
TCGAAAATCGTTGCTCCTGAGAAGCCCTTGGCTCTTCATTCAGCCAAGGATTCTCCACCT
ATTCAGAACAATGAAGCTAAGACTGAAGACACACCTGTACTCTCGACTGTTCAGCCCGTC
AATGGATTTTCAACTATTCAGCCCGTCAATGGACCTTCAGCTGTTCAGCCCGTCAATGGA
CCTTTGGCTGTTCAGCCTGTCAATGGACCTTCGGCTCTTCAGCCCGTCAATGGACCTTCG
GCCGTAATTGTCCCGGTACAAGCTGATGAAATTAAAAAACCTTCAACACCTCCTAAAAGC
ATTTCTAGTAAGGTGGGAGTTATGATGAAAATGAGTTCACAAACTATTCTCAAGAATTGC
AAGAGAAAACAGATTGATTGGCATGTACCACCAGGAATGGAACTTGACGAACTCTGGAGA
GTAGCCGCTGGTGGTAATAGCAAGGAGGCTGATGTTCAGAGAAACAGAAACCGGCGAGAA
AGAGAAACAACATATCAGTCTCTTCAAACTATACCGTTGAACCCTAAAGAACCATGGGAT
AGGGAAATGGACTATGATGACAGTTTGACCCCTGAAATTCCATCTCAACAGCCACCAGAA
GAAAGTTTAACGGAACCACAGGATTCACTTGATGAACGAAGAATTGCTGCTGGTGCTGCC
ACAACCTCTTCATCTCTAAGCAGTCCTGAACCTGATCTCGAGTTATTAGCTGCGTTACTT
AAGAACCCAGATCTTGTTTATGCACTAACTTCGGGAAAACCCAGTAATTTAGCCGGCCAA
GATATGGTAAAACTGCTTGATGTGATTAAGACTGGTGCACCAAACTCAAGCAGTAGCTCA
AATAAACAGGTTGAAGAAAGGGTCGAAGTTTCCCTTCCATCTCCCACTCCATCAACTAAT
CCTGGAATGAGTGGATGGGGACAAGAAGGGATTCGGAATCCATTTTCAAGGCAAAACCAA
GTTGGTACTGCAGTTGCTAGATCGGGTACACAGCTTCGTGTTGGTTCAATGCAATGGCAT
CAAACAAATGAACAATCAATCCCACGACATGCTCCATCAGCATACAGTAACTCGATCACA
TTGGCTCACACAGAAAGAGAACAGCAACAATATATGCAACCAAAACTTCATCACAATTTA
CATTTTCAACAACAACAACAACAACCAATCTCAACAACCTCGTATGCAGTTAGGGAACCA
GTAGGACAAATGGGAACAGGTACATCGAGTTCATGGAGGAGTCAGCAGAGTCAGAACAGT
TACTACTCACATCAAGAAAACGAGATTGCATCGGCTTCACAAGTTACTTCATACCAAGGG
AATAGCCAGTACATGAGTAGCAATCCAGGATATGAATCATGGAGTCCTGATAATAGCCCA
AGTAGGAACCAGCTTAACATGAGGGGACAACAACAACAAGCATCAAGGAAACATGATTCT
TCTACTCATCCATATTGGAACCAAAACAAAAGATGGCGTTAA


Protein Translation:


MDAFKEEIEIGSSVESLMELLDSQKVLFHSQIDQLQDVVVAQCKLTGVNPLAQEMAAGAL
SIKIGKRPRDLLNPKAVKYLQAVFAIKDAISKRESREISALFGITVAQVREFFVTQKTRV
RKQVRLSREKVVMSNTHALQDDGVPENNNATNHVEPVPLNSIHPEACSISWGEGETVALI
PPEDIPPDISDSDKYFVENIFSLLRKEETFSGQVKLMEWIMQIQDASVLIWFLSKGGVLI
LTTWLSQAASEEQTSVLLLILKVLCHLPLHKASPENMSAILQSVNGLRFYRISDISNRAK
GLLSRWTKLFAKIQAMKKQNRNSSQIDSQSQLLLKQSIAEIMGDSSNPEDILSLSNGKSE
NVRRIESSQGPKLLLTSADDSTKKHMLGSNPSYNKERRKVQMVEQPGQKAAGKSPQTVRI
GTSGRSRPMSADDIQKAKMRALYMQSKNSKKDPLPSAIGDSKIVAPEKPLALHSAKDSPP
IQNNEAKTEDTPVLSTVQPVNGFSTIQPVNGPSAVQPVNGPLAVQPVNGPSALQPVNGPS
AVIVPVQADEIKKPSTPPKSISSKVGVMMKMSSQTILKNCKRKQIDWHVPPGMELDELWR
VAAGGNSKEADVQRNRNRRERETTYQSLQTIPLNPKEPWDREMDYDDSLTPEIPSQQPPE
ESLTEPQDSLDERRIAAGAATTSSSLSSPEPDLELLAALLKNPDLVYALTSGKPSNLAGQ
DMVKLLDVIKTGAPNSSSSSNKQVEERVEVSLPSPTPSTNPGMSGWGQEGIRNPFSRQNQ
VGTAVARSGTQLRVGSMQWHQTNEQSIPRHAPSAYSNSITLAHTEREQQQYMQPKLHHNL
HFQQQQQQPISTTSYAVREPVGQMGTGTSSSWRSQQSQNSYYSHQENEIASASQVTSYQG
NSQYMSSNPGYESWSPDNSPSRNQLNMRGQQQQASRKHDSSTHPYWNQNKRWR*

Protein motifs:

There are a number of interesting features to the LD protein sequence: a putative ATP/GTP-binding (P-loop) motif, two putative bipartite nuclear localization signals, a glutamine-rich domain (found in several transcription factors), five tandem copies of a nonapeptide repeat, and a putative homeodomain. Please see the article by Lee, et al. for a discussion of these motifs.

P-loop:   407  GQKAAGKS  414

NLS1:   383  KKxxxxxxxxxxKERRK  399

NLS2:   936  RKxxxxxxxxxxxxKRWR  953

glutamine-rich domain:   828 to 933

nonapeptide repeat:   494  VQPVNGFST
                           IQPVNGPSA
                           VQPVNGPLA
                           VQPVNGPSA
                           LQPVNGPSA  541

putative homeodomain:  65  GKRPRDLLNPKAVKYLQAVFAIKDAISKRE
                           SREISALFGITVAQVREFFVTQKTRVRKQV  124

 


written 12 Aug 97
updated 10 Oct 97
updated 16 Oct 97
updated 17 Oct 97
updated 19 Jun 98
Larry Parnell